Canonical Allele Identifier: PA2825056057
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2450923
ClinVar RCV Id: RCV003177300
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val449Leu
CA374106263
NM_000136.3:c.1345G>T
CA374106264
NM_000136.3:c.1345G>C