Canonical Allele Identifier: PA166939
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg331Gln
CA023399
NM_000455.5:c.992G>A