Canonical Allele Identifier: PA2825056247
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2092843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ser543Leu
CA374104373
NM_000136.3:c.1628C>T