Canonical Allele Identifier: PA916046333
Gene: STING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 475208
ClinVar RCV Id: RCV000539383 RCV001092019 RCV002263800 RCV003905453 RCV004024307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354187.1:p.Gly73Val
CA3435365
NM_001367258.1:c.218G>T