Canonical Allele Identifier: PA915964932
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 663449
ClinVar RCV Id: RCV000821318 RCV004029065 RCV002290469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Glu866Asp
CA401326321
NM_001079804.3:c.2598A>C
CA401326323
NM_001079804.3:c.2598A>T