Canonical Allele Identifier: PA196887
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 187158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro411Ala
CA022510
NM_000455.5:c.1231C>G