Canonical Allele Identifier: PA2828304895
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 559301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355929.1:p.Tyr129Cys
CA192400994
NM_001369000.1:c.386A>G