Allele Registry

Canonical Allele Identifier: PA120121

Gene: GCNT2 HGNC NCBI

ClinVar RCV:

RCV000009699

ClinVar Variation:

9128

HGVS (amino-acid)	Matching Registered Transcripts
NP_663630.2:p.Gly350Glu	CA120118 NM_145655.3:c.1049G>A