Allele Registry

Canonical Allele Identifier: PA093471

Gene: SI HGNC NCBI

ClinVar RCV:

RCV000001478

ClinVar Variation:

1413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032.2:p.Leu341Pro	CA115000 NM_001041.4:c.1022T>C