Canonical Allele Identifier: PA2828304299
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 994780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355924.1:p.Ala198Val
CA5022363
NM_001368995.1:c.593C>T