Canonical Allele Identifier: PA916006643
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 802491
ClinVar RCV Id: RCV000988192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg542Lys
CA374104397
NM_001243743.2:c.1625G>A