Canonical Allele Identifier: PA300042
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 182920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg425His
CA022577
NM_000455.5:c.1274G>A