Canonical Allele Identifier: PA1139694195
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 945288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Glu539Lys
CA374104458
NM_001243743.2:c.1615G>A