Allele Registry

Canonical Allele Identifier: PA093525

Gene: SI HGNC NCBI

ClinVar RCV:

RCV000001483

RCV000481721

RCV003415621

ClinVar Variation:

1418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032.2:p.Val577Gly	CA115005 NM_001041.4:c.1730T>G