Canonical Allele Identifier: PA915964467
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4036
ClinVar Variation Id: 1324438
ClinVar RCV Id: RCV001781143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Gly293Arg
CA116622
NM_001079804.3:c.877G>A
CA401363876
NM_001079804.3:c.877G>C