Canonical Allele Identifier: PA916006624
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216285
ClinVar RCV Id: RCV000199976 RCV000520121 RCV001167954 RCV001012322 RCV003153471
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Arg532Lys
CA339012
NM_001243743.2:c.1595G>A