Allele Registry

Canonical Allele Identifier: PA120119

Gene: GCNT2 HGNC NCBI

ClinVar RCV:

RCV000009699

ClinVar Variation:

9128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001482.1:p.Gly348Glu	CA120118 NM_001491.3:c.1043G>A