Canonical Allele Identifier: PA2573176622
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1359350
ClinVar RCV Id: RCV001904391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Tyr366Ser
CA401364945
NM_001079804.3:c.1097A>C