Canonical Allele Identifier: PA2825065078
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_000143.2:p.Lys162Arg
CA401361638
NM_000152.5:c.485A>G