Canonical Allele Identifier: PA2580176486
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1774754
ClinVar RCV Id: RCV002403078
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala513Val
CA374104852
NM_001243743.2:c.1538C>T