Canonical Allele Identifier: PA1139694497
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 941385
ClinVar RCV Id: RCV001211164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Arg162Thr
CA374338619
NM_001243744.2:c.485G>C