Canonical Allele Identifier: PA2825143998
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753952
ClinVar RCV Id: RCV002364166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro217Arg
CA402949619
NM_000455.5:c.650C>G