Canonical Allele Identifier: PA2826331728
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1768973
ClinVar RCV Id: RCV002383190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Tyr429Phe
CA374107306
NM_001243743.2:c.1286A>T