Canonical Allele Identifier: PA2825461764
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 849167
ClinVar RCV Id: RCV001053072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Asn520Ser
CA401367197
NM_001079803.3:c.1559A>G