Canonical Allele Identifier: PA189559
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184646
ClinVar RCV Id: RCV000163934 RCV000234273 RCV000486365 RCV000657114 RCV001262270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala398Val
CA022442
NM_000455.5:c.1193C>T