Canonical Allele Identifier: PA2825056246
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 802491
ClinVar RCV Id: RCV000988192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg542Lys
CA374104397
NM_000136.3:c.1625G>A