Allele Registry

Canonical Allele Identifier: PA093451

Gene: SI HGNC NCBI

ClinVar RCV:

RCV000001479

ClinVar Variation:

1414

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032.2:p.Gln117Arg	CA115001 NM_001041.4:c.350A>G