Canonical Allele Identifier: PA891845657
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 565797
ClinVar RCV Id: RCV000685442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Thr151Ile
CA401361472
NM_000152.5:c.452C>T