Canonical Allele Identifier: PA2825444139
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1714754
ClinVar RCV Id: RCV002299121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asn882Ser
CA401326499
NM_001079804.3:c.2645A>G