Allele Registry

Canonical Allele Identifier: PA916076801

Gene: GCNT2 HGNC NCBI

ClinVar RCV:

RCV000870741

RCV002292591

ClinVar Variation:

701963

HGVS (amino-acid)	Matching Registered Transcripts
NP_663630.2:p.Ala169Thr	CA3632232 NM_145655.3:c.505G>A