Allele Registry

Canonical Allele Identifier: PA2826976872

Gene: A4GALT HGNC NCBI

ClinVar RCV:

RCV002508135

ClinVar Variation:

39437

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304967.1:p.Gln211Glu	CA130289 NM_001318038.3:c.631C>G