Canonical Allele Identifier: PA645459836
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428790
ClinVar RCV Id: RCV000492488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Leu182Arg
CA402949116
NM_000455.5:c.545T>G