Canonical Allele Identifier: PA915964684
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 660436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Gly532Ser
CA8815388
NM_001079804.3:c.1594G>A