Allele Registry

Canonical Allele Identifier: PA2826976897

Gene: A4GALT HGNC NCBI

ClinVar RCV:

RCV001889044

ClinVar Variation:

1385893

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304967.1:p.Arg340Cys	CA10270160 NM_001318038.3:c.1018C>T