Canonical Allele Identifier: PA645402644
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 419389
ClinVar RCV Id: RCV000483173 RCV000806505 RCV002374890
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Cys387Arg
CA16618880
NM_000136.3:c.1159T>C