Canonical Allele Identifier: PA645459764
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403766
ClinVar RCV Id: RCV000474390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro38Thr
CA16616001
NM_000455.5:c.112C>A