Canonical Allele Identifier: PA915964196
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asp91Asn
CA116586
NM_001079804.3:c.271G>A