Canonical Allele Identifier: PA2573176452
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1511437
ClinVar RCV Id: RCV002043328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ala17Ser
CA401360048
NM_001079804.3:c.49G>T