Canonical Allele Identifier: PA2825065041
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1516069
ClinVar RCV Id: RCV002048680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser143Ala
CA401361278
NM_000152.5:c.427T>G