Allele Registry

Canonical Allele Identifier: PA108983

Gene: STING1 HGNC NCBI

ClinVar RCV:

RCV000133400

ClinVar Variation:

143861

HGVS (amino-acid)	Matching Registered Transcripts
NP_938023.1:p.Asn154Ser	CA170516 NM_198282.4:c.461A>G