Canonical Allele Identifier: PA645481932
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 291139
ClinVar RCV Id: RCV000278660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp741Val
CA10607034
NM_000152.5:c.2222A>T