Canonical Allele Identifier: PA2580176461
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1771561
ClinVar RCV Id: RCV002396695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala464Val
CA374106146
NM_001243743.2:c.1391C>T