Canonical Allele Identifier: PA2825065608
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 991138
ClinVar RCV Id: RCV001279298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Arg411Trp
CA8815240
NM_000152.5:c.1231C>T