Canonical Allele Identifier: PA645377270
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 286950
ClinVar RCV Id: RCV000351313
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_778243.1:p.Arg318His
CA5022242
NM_175073.3:c.953G>A