NM_017849.4(TMEM127):c.468C>A (p.Ala156=) AND Hereditary pheochromocytoma-paraganglioma
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000933167.8
Allele description
NM_017849.4(TMEM127):c.468C>A (p.Ala156=)
Condition(s)
- Name:
- Hereditary pheochromocytoma-paraganglioma
- Synonyms:
- Hereditary Paraganglioma-Pheochromocytoma Syndromes; Hereditary Paragangliomas and Pheochromocytomas
- Identifiers:
- MONDO: MONDO:0017366; MedGen: C1708353
-
Homo sapiens prolyl 4-hydroxylase subunit alpha 2 (P4HA2), transcript variant 1,...
Homo sapiens prolyl 4-hydroxylase subunit alpha 2 (P4HA2), transcript variant 1, mRNAgi|1724241252|ref|NM_004199.3|Nucleotide
-
ST42eORF042 [Staphylococcus phage 42E]
ST42eORF042 [Staphylococcus phage 42E]Gene ID:5133007Gene
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Last Updated: May 1, 2024