Canonical Allele Identifier: PA913192961
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 630002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp359Glu
CA402951894
NM_000455.5:c.1077C>A
CA402951895
NM_000455.5:c.1077C>G