Canonical Allele Identifier: PA2825064955
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1370286
ClinVar RCV Id: RCV001899296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp91Tyr
CA8814836
NM_000152.5:c.271G>T