Canonical Allele Identifier: PA113175
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2736677
ClinVar RCV Id: RCV003502028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Glu521Gln
CA401367201
NM_000152.5:c.1561G>C