Canonical Allele Identifier: PA113339
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4023
ClinVar RCV Id: RCV000004238 RCV000409137 RCV000788193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly643Arg
CA116596
NM_000152.5:c.1927G>A
CA401369898
NM_000152.5:c.1927G>C