Allele Registry

Canonical Allele Identifier: PA2573269578

Gene: A4GALT HGNC NCBI

ClinVar RCV:

RCV001974824

ClinVar Variation:

1438947

HGVS (amino-acid)	Matching Registered Transcripts
NP_059132.1:p.Thr210Pro	CA10270252 NM_017436.7:c.628A>C