Canonical Allele Identifier: PA1139669354
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 856981
ClinVar RCV Id: RCV001062565

Amino-acid Alleles

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