Allele Registry

Canonical Allele Identifier: PA658831914

Gene: GNPTG HGNC NCBI

ClinVar RCV:

RCV000664475

RCV002530627

ClinVar Variation:

549903

HGVS (amino-acid)	Matching Registered Transcripts
NP_115909.1:p.Ala25Gly	CA394184063 NM_032520.5:c.74C>G