Canonical Allele Identifier: PA2825143104
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1746937
ClinVar RCV Id: RCV002346897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg40Leu
CA402943942
NM_000455.5:c.119G>T