Canonical Allele Identifier: PA2580176487
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.His514Gln
CA374104837
NM_001243743.2:c.1542C>G
CA374104839
NM_001243743.2:c.1542C>A