Canonical Allele Identifier: PA645459962
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 412537
ClinVar Variation Id: 2774544
ClinVar RCV Id: RCV003585835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Glu357Asp
CA045047
NM_000455.5:c.1071G>T
CA402951874
NM_000455.5:c.1071G>C