Allele Registry

Canonical Allele Identifier: PA1139669354

Gene: STK11 HGNC NCBI

ClinVar RCV:

RCV001062565

ClinVar Variation:

856981

HGVS (amino-acid)	Matching Registered Transcripts
NP_000446.1:p.Lys97Asn	CA402947617 NM_000455.5:c.291G>C CA402947619 NM_000455.5:c.291G>T