Canonical Allele Identifier: PA2826865590
Gene: STING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 143863
ClinVar RCV Id: RCV000133402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288667.1:p.Val147Leu
CA170518
NM_001301738.1:c.439G>C
CA361481088
NM_001301738.1:c.439G>T