Canonical Allele Identifier: PA2825055214
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1776998
ClinVar RCV Id: RCV002403519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met55Val
CA374340188
NM_000136.3:c.163A>G