Allele Registry

Canonical Allele Identifier: PA916046330

Gene: STING1 HGNC NCBI

ClinVar RCV:

RCV000133401

RCV000481634

ClinVar Variation:

143862

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354187.1:p.Val36Met	CA170517 NM_001367258.1:c.106G>A