Canonical Allele Identifier: PA165652
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Val150Ala
CA022959
NM_000455.5:c.449T>C