Canonical Allele Identifier: PA915964171
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 580689
ClinVar RCV Id: RCV000704307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ala77Ser
CA401360496
NM_001079804.3:c.229G>T