Allele Registry

Canonical Allele Identifier: PA093461

Gene: SI HGNC NCBI

ClinVar RCV:

RCV000001484

RCV000622702

RCV001324096

ClinVar Variation:

1419

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032.2:p.Gly1073Asp	CA115006 NM_001041.4:c.3218G>A