Canonical Allele Identifier: PA915964522
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 555820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Trp367Arg
CA401364950
NM_001079804.3:c.1099T>A
CA401364951
NM_001079804.3:c.1099T>C