Canonical Allele Identifier: PA2741845417
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2585975
ClinVar RCV Id: RCV003358185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ile538Val
CA374104474
NM_001243743.2:c.1612A>G