Canonical Allele Identifier: PA111049
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 7458
ClinVar RCV Id: RCV000007884
ClinVar Variation Id: 801286
ClinVar RCV Id: RCV000986039
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Trp239Cys
CA023239
NM_000455.5:c.717G>C
CA402949935
NM_000455.5:c.717G>T