NM_138694.4(PKHD1):c.10893T>C (p.Tyr3631=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000592861.4
Allele description [Variation Report for NM_138694.4(PKHD1):c.10893T>C (p.Tyr3631=)]
NM_138694.4(PKHD1):c.10893T>C (p.Tyr3631=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
replication factor C subunit 2 isoform 5 [Homo sapiens]
replication factor C subunit 2 isoform 5 [Homo sapiens]gi|525343614|ref|NP_001265722.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024