Canonical Allele Identifier: PA2825463513
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 526538
ClinVar RCV Id: RCV000631088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Val921Phe
CA401327245
NM_001079803.3:c.2761G>T