Canonical Allele Identifier: PA2826865593
Gene: STING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 143861
ClinVar RCV Id: RCV000133400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288667.1:p.Asn154Ser
CA170516
NM_001301738.1:c.461A>G