Canonical Allele Identifier: PA2825459800
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1370286
ClinVar RCV Id: RCV001899296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Asp91Tyr
CA8814836
NM_001079803.3:c.271G>T