Canonical Allele Identifier: PA2828305279
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 1302141
ClinVar RCV Id: RCV001754030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355933.1:p.Arg111Cys
CA5022362
NM_001369004.1:c.331C>T