Allele Registry

Canonical Allele Identifier: PA2826976871

Gene: A4GALT HGNC NCBI

ClinVar RCV:

RCV001974824

ClinVar Variation:

1438947

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304967.1:p.Thr210Pro	CA10270252 NM_001318038.3:c.628A>C