Canonical Allele Identifier: PA169439
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142798
ClinVar RCV Id: RCV000132217 RCV001043772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile356Met
CA022258
NM_000455.5:c.1068C>G