Canonical Allele Identifier: PA113207
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 189065
ClinVar RCV Id: RCV000169462 RCV000481943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly219Arg
CA274334
NM_000152.5:c.655G>A
CA401362459
NM_000152.5:c.655G>C