Canonical Allele Identifier: PA645459978
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 237789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala377Pro
CA045509
NM_000455.5:c.1129G>C