Canonical Allele Identifier: PA891845676
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 575986
ClinVar RCV Id: RCV000698352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro266Leu
CA401363498
NM_000152.5:c.797C>T