Allele Registry

Canonical Allele Identifier: PA645466126

Gene: B3GALNT2 HGNC NCBI

ClinVar RCV:

RCV000490097

ClinVar Variation:

427099

HGVS (amino-acid)	Matching Registered Transcripts
NP_689703.1:p.Gly248Ala	CA1464816 NM_152490.5:c.743G>C