Allele Registry

Canonical Allele Identifier: PA191322

Gene: STK11 HGNC NCBI

ClinVar RCV:

RCV000164582

RCV001808439

ClinVar Variation:

185210

HGVS (amino-acid)	Matching Registered Transcripts
NP_000446.1:p.Gln137Lys	CA022909 NM_000455.5:c.409C>A