Canonical Allele Identifier: PA167738
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142198
ClinVar RCV Id: RCV000131186 RCV000168376 RCV000222337 RCV000765433 RCV001354464 RCV002243796 RCV003407552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Val338Met
CA022150
NM_000455.5:c.1012G>A