Canonical Allele Identifier: PA1139671077
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_001073272.1:p.Arg411Trp
CA8815240
NM_001079804.3:c.1231C>T