Canonical Allele Identifier: PA113585
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 556117
ClinVar RCV Id: RCV000672072 RCV001549927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro266Ser
CA401363495
NM_000152.5:c.796C>T