Canonical Allele Identifier: PA2825056231
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1983431
ClinVar RCV Id: RCV002770267
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gly537Val
CA5137291
NM_000136.3:c.1610G>T