Canonical Allele Identifier: PA891850074
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 568685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile267Val
CA402950551
NM_000455.5:c.799A>G