Canonical Allele Identifier: PA916007113
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 526383
ClinVar RCV Id: RCV000630907 RCV001017222
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Arg361Gln
CA5137460
NM_001243744.2:c.1082G>A