Allele Registry

Canonical Allele Identifier: PA234049

Gene: GAA HGNC NCBI

ClinVar RCV:

RCV000153288

RCV001326695

ClinVar Variation:

167112

HGVS (amino-acid)	Matching Registered Transcripts
NP_000143.2:p.Tyr407His	CA234047 NM_000152.5:c.1219T>C