Canonical Allele Identifier: PA2825461502
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2862966
ClinVar RCV Id: RCV003609110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Pro457Ser
CA401366410
NM_001079803.3:c.1369C>T