Canonical Allele Identifier: PA109001
Gene: STING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 143862
ClinVar RCV Id: RCV000133401 RCV000481634
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Amino-acid Alleles

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