Canonical Allele Identifier: PA2825056085
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1771561
ClinVar RCV Id: RCV002396695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ala464Val
CA374106146
NM_000136.3:c.1391C>T