Canonical Allele Identifier: PA2825460709
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1373977
ClinVar RCV Id: RCV001877587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.His295Tyr
CA401363899
NM_001079803.3:c.883C>T