Allele Registry

Canonical Allele Identifier: PA284848

Gene: GNPTG HGNC NCBI

ClinVar RCV:

RCV000058938

ClinVar Variation:

68109

HGVS (amino-acid)	Matching Registered Transcripts
NP_115909.1:p.Leu230Val	CA284847 NM_032520.5:c.688C>G