Canonical Allele Identifier: PA658670264
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 485001
ClinVar RCV Id: RCV000572383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Lys178Thr
CA402949063
NM_000455.5:c.533A>C