Canonical Allele Identifier: PA113234
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 972790
ClinVar RCV Id: RCV001249005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Gly335Arg
CA501005
NM_000152.5:c.1003G>A
CA401364542
NM_000152.5:c.1003G>C