Canonical Allele Identifier: PA2741845396
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2585978
ClinVar RCV Id: RCV003368119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Leu479Pro
CA374105935
NM_001243743.2:c.1436T>C