Canonical Allele Identifier: PA915964495
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met318Thr
CA116590
NM_001079804.3:c.953T>C