Canonical Allele Identifier: PA2825462503
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 656668
ClinVar RCV Id: RCV000813141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Ser686Lys
CA915952255
NM_001079803.3:c.2057_2058delinsAA