Canonical Allele Identifier: PA2825143752
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2746064
ClinVar RCV Id: RCV003506887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Phe157Val
CA402948785
NM_000455.5:c.469T>G