Canonical Allele Identifier: PA169821
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142939
ClinVar RCV Id: RCV000132421 RCV000197228 RCV000222146 RCV002267886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr367Met
CA022292
NM_000455.5:c.1100C>T