Canonical Allele Identifier: PA891850121
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 576503
ClinVar RCV Id: RCV000699013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile360Thr
CA402951903
NM_000455.5:c.1079T>C