Canonical Allele Identifier: PA916006647
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Lys545Glu
CA16618872
NM_001243743.2:c.1633A>G