Canonical Allele Identifier: PA1139670467
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 842137
ClinVar RCV Id: RCV001044505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Phe128Ser
CA401360986
NM_001079804.3:c.383T>C