Canonical Allele Identifier: PA113558
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1067893
ClinVar RCV Id: RCV001379276 RCV002223308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Met519Val
CA401367186
NM_000152.5:c.1555A>G