Allele Registry

Canonical Allele Identifier: PA916046329

Gene: STING1 HGNC NCBI

ClinVar RCV:

RCV000133400

ClinVar Variation:

143861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354187.1:p.Asn35Ser	CA170516 NM_001367258.1:c.104A>G