Canonical Allele Identifier: PA2826865443
Gene: STING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 541983
ClinVar RCV Id: RCV000762166 RCV001080030 RCV002263913 RCV003905771 RCV004025853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288667.1:p.Ala21Thr
CA3435506
NM_001301738.1:c.61G>A