Canonical Allele Identifier: PA2825464035
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2138931
ClinVar RCV Id: RCV003066465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Lys162Arg
CA401361638
NM_001079804.3:c.485A>G