Canonical Allele Identifier: PA2825443767
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2874367
ClinVar RCV Id: RCV003610604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Tyr766His
CA401324883
NM_001079804.3:c.2296T>C