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
CA022756
NM_000455.5:c.250A>T
CA402944469
NM_000455.5:c.241A>T
CA402944482
NM_000455.5:c.244A>T
CA402944496
NM_000455.5:c.247A>T