Canonical Allele Identifier: PA916006952
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182474
ClinVar RCV Id: RCV000160475 RCV001025356 RCV000791796 RCV001358559
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Pro217Leu
CA299151
NM_001243744.2:c.650C>T