Allele Registry

Canonical Allele Identifier: PA093442

Gene: SI HGNC NCBI

ClinVar RCV:

RCV000001477

RCV002512643

ClinVar Variation:

1412

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032.2:p.Gln1098Pro	CA114999 NM_001041.4:c.3293A>C