Canonical Allele Identifier: PA915964868
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 499293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Trp746Arg
CA401324768
NM_001079804.3:c.2236T>A
CA401324769
NM_001079804.3:c.2236T>C