Canonical Allele Identifier: PA1139670504
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 892321
ClinVar RCV Id: RCV001128258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Glu145Asp
CA8814872
NM_001079804.3:c.435A>T
CA401361335
NM_001079804.3:c.435A>C