Canonical Allele Identifier: PA645459874
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 378676
ClinVar Variation Id: 826850
ClinVar RCV Id: RCV001026060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp237Glu
CA16608016
NM_000455.5:c.711C>G
CA402949910
NM_000455.5:c.711C>A