Canonical Allele Identifier: PA2580176616
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1728901
ClinVar RCV Id: RCV002323037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Gln107Arg
CA374339247
NM_001243744.2:c.320A>G