Canonical Allele Identifier: PA913191899
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 596014
ClinVar RCV Id: RCV000731715 RCV001243448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Thr23Ala
CA8814777
NM_000152.5:c.67A>G