Canonical Allele Identifier: PA2826331340
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456149
ClinVar RCV Id: RCV000549299 RCV002384041
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Thr344Ala
CA374108173
NM_001243743.2:c.1030A>G