Canonical Allele Identifier: PA162201
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 7461
ClinVar Variation Id: 376711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Phe354Leu
CA022247
NM_000455.5:c.1062C>G
CA16603121
NM_000455.5:c.1060T>C
CA402951852
NM_000455.5:c.1062C>A