NM_001375505.1(MAP2):c.1895C>T (p.Ala632Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004416144.1
Allele description [Variation Report for NM_001375505.1(MAP2):c.1895C>T (p.Ala632Val)]
NM_001375505.1(MAP2):c.1895C>T (p.Ala632Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
la-related protein 4 isoform X19 [Homo sapiens]
la-related protein 4 isoform X19 [Homo sapiens]gi|2217287252|ref|XP_047284189.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024