Allele Registry

Canonical Allele Identifier: PA097708

Gene: HS6ST1 HGNC NCBI

ClinVar RCV:

RCV000032891

RCV000156968

RCV000455725

RCV001258243

RCV001358502

RCV003917537

ClinVar Variation:

180161

HGVS (amino-acid)	Matching Registered Transcripts
NP_004798.3:p.Arg382Trp	CA185895 NM_004807.3:c.1144C>T