Canonical Allele Identifier: PA2499237167
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1020834
ClinVar RCV Id: RCV001320484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asn815Thr
CA401325230
NM_001079804.3:c.2444A>C