Canonical Allele Identifier: PA186531
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 183802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg304Trp
CA023348
NM_000455.5:c.910C>T