Canonical Allele Identifier: PA164387
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro326Leu
CA023393
NM_000455.5:c.977C>T