Canonical Allele Identifier: PA2741817921
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2702387
ClinVar RCV Id: RCV003508012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Gln399Arg
CA402953655
NM_000455.5:c.1196A>G