Canonical Allele Identifier: PA113482
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 284093
ClinVar RCV Id: RCV000353485 RCV000725389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Leu355Pro
CA8815136
NM_000152.5:c.1064T>C