Canonical Allele Identifier: PA116603
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4025
ClinVar RCV Id: RCV000004240 RCV000795023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Leu299Arg
CA116601
NM_001079803.3:c.896T>G