Canonical Allele Identifier: PA645481469
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 283636
ClinVar RCV Id: RCV000345427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser9Pro
CA10604542
NM_000152.5:c.25T>C