Canonical Allele Identifier: PA2826200276
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 994780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182181.2:p.Ala126Val
CA5022363
NM_001195252.2:c.377C>T