Canonical Allele Identifier: PA2828305391
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 214121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355934.1:p.Arg157His
CA319960
NM_001369005.1:c.470G>A