Canonical Allele Identifier: PA2825462610
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 381006
ClinVar Variation Id: 456391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Thr711Arg
CA8815620
NM_001079803.3:c.2132C>G
CA658658713
NM_001079803.3:c.2132_2133delinsGG