Allele Registry

Canonical Allele Identifier: PA284846

Gene: GNPTG HGNC NCBI

ClinVar RCV:

RCV000058937

RCV000665994

RCV003488372

ClinVar Variation:

68108

HGVS (amino-acid)	Matching Registered Transcripts
NP_115909.1:p.Ala25Glu	CA284845 NM_032520.5:c.74C>A