Canonical Allele Identifier: PA2826200192
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 994780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182180.1:p.Ala198Val
CA5022363
NM_001195251.2:c.593C>T