Canonical Allele Identifier: PA2825143076
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1797410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Gln37His
CA402943895
NM_000455.5:c.111G>T
CA402943900
NM_000455.5:c.111G>C