Allele Registry

Canonical Allele Identifier: PA109001

Gene: STING1 HGNC NCBI

ClinVar RCV:

RCV000133401

RCV000481634

ClinVar Variation:

143862

HGVS (amino-acid)	Matching Registered Transcripts
NP_938023.1:p.Val155Met	CA170517 NM_198282.4:c.463G>A