Canonical Allele Identifier: PA658826232
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 552776
ClinVar RCV Id: RCV000668100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asp406Asn
CA401365200
NM_000152.5:c.1216G>A