Canonical Allele Identifier: PA2825056089
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1771958
ClinVar RCV Id: RCV002389435
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val470Ile
CA374106074
NM_000136.3:c.1408G>A