Canonical Allele Identifier: PA2825459880
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 847865
ClinVar RCV Id: RCV001051500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Cys108Ser
CA401360738
NM_001079803.3:c.322T>A
CA401360745
NM_001079803.3:c.323G>C