Canonical Allele Identifier: PA166602
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Lys84del
CA022751
NM_000455.5:c.250_252del