Canonical Allele Identifier: PA658670109
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 458049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Leu17Val
CA047985
NM_000455.5:c.49C>G