Allele Registry

Canonical Allele Identifier: PA093480

Gene: SI HGNC NCBI

ClinVar RCV:

RCV000001480

ClinVar Variation:

1415

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032.2:p.Leu620Pro	CA115002 NM_001041.4:c.1859T>C