Canonical Allele Identifier: PA915964771
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_001073272.1:p.Gly643Arg
CA116596
NM_001079804.3:c.1927G>A
CA401369898
NM_001079804.3:c.1927G>C