Canonical Allele Identifier: PA891849933
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 584981
ClinVar RCV Id: RCV000709571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Val63Ala
CA402944244
NM_000455.5:c.188T>C