Canonical Allele Identifier: PA2828305238
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_001355932.1:p.Arg230His
CA5022242
NM_001369003.1:c.689G>A