Canonical Allele Identifier: PA2580176489
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1774945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala516Thr
CA374104823
NM_001243743.2:c.1546G>A