Canonical Allele Identifier: PA658826229
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 555820
ClinVar RCV Id: RCV000671718 RCV001785699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp367Arg
CA401364950
NM_000152.5:c.1099T>A
CA401364951
NM_000152.5:c.1099T>C