Canonical Allele Identifier: PA2826330573
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1329751
ClinVar RCV Id: RCV001800059 RCV002334701
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Val154Gly
CA374338666
NM_001243743.2:c.461T>G