Canonical Allele Identifier: PA2825461787
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4026
ClinVar RCV Id: RCV000004241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Ser529Val
CA116604
NM_001079803.3:c.1585_1586delinsGT