Canonical Allele Identifier: PA2580176754
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760094
ClinVar RCV Id: RCV002400470
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.His256Pro
CA374109332
NM_001243744.2:c.767A>C