Allele Registry

Canonical Allele Identifier: PA2741962659

Gene: A4GALT HGNC NCBI

ClinVar RCV:

RCV004294097

ClinVar Variation:

2516437

HGVS (amino-acid)	Matching Registered Transcripts
NP_059132.1:p.Tyr341Cys	CA10270157 NM_017436.7:c.1022A>G