Canonical Allele Identifier: PA2825056235
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2585975
ClinVar RCV Id: RCV003358185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile538Val
CA374104474
NM_000136.3:c.1612A>G