Canonical Allele Identifier: PA167970
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142292
ClinVar RCV Id: RCV000131326 RCV000197480 RCV000487216 RCV000657038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg409Gln
CA022499
NM_000455.5:c.1226G>A