Canonical Allele Identifier: PA2825460766
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.His308Tyr
CA8815089
NM_001079803.3:c.922C>T