Canonical Allele Identifier: PA658670158
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 458024
ClinVar RCV Id: RCV000528814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Lys41Thr
CA402943954
NM_000455.5:c.122A>C