Canonical Allele Identifier: PA645481850
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 371226
ClinVar RCV Id: RCV000409030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly611Asp
CA16041897
NM_000152.5:c.1832G>A