Canonical Allele Identifier: PA645459968
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 419166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr363Ala
CA045091
NM_000455.5:c.1087A>G