Canonical Allele Identifier: PA2580176508
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2092843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ser543Leu
CA374104373
NM_001243743.2:c.1628C>T