Canonical Allele Identifier: PA1139670373
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 940369
ClinVar RCV Id: RCV001209942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp358Gly
CA045065
NM_000455.5:c.1073A>G