Canonical Allele Identifier: PA2826331084
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2785117
ClinVar RCV Id: RCV003636171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ile276Thr
CA374109201
NM_001243743.2:c.827T>C