Canonical Allele Identifier: PA916007142
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 550052
ClinVar RCV Id: RCV000664675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Trp403Arg
CA374107473
NM_001243744.2:c.1207T>C
CA374107474
NM_001243744.2:c.1207T>A