Canonical Allele Identifier: PA2825056186
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2450926
ClinVar RCV Id: RCV003177302
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ile518Val
CA374104791
NM_000136.3:c.1552A>G