Canonical Allele Identifier: PA913192939
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 628399
ClinVar RCV Id: RCV000772860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala318Val
CA402951526
NM_000455.5:c.953C>T