Canonical Allele Identifier: PA2825066334
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1524086
ClinVar RCV Id: RCV002031456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly747Trp
CA294856500
NM_000152.5:c.2239G>T