Canonical Allele Identifier: PA1139671027
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 839690
ClinVar RCV Id: RCV001041506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ala394Thr
CA294892303
NM_001079804.3:c.1180G>A