Allele Registry

Canonical Allele Identifier: PA188229

Gene: STK11 HGNC NCBI

ClinVar Allele:

185541

ClinVar RCV:

RCV000163414

RCV000587411

RCV000811562

RCV003230423

ClinVar Variation:

184219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000446.1:p.Gly381Ala	CA022351 NM_000455.5:c.1142G>C