Canonical Allele Identifier: PA916046329
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_001354187.1:p.Asn35Ser
CA170516
NM_001367258.1:c.104A>G