Canonical Allele Identifier: PA891850008
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 571305
ClinVar RCV Id: RCV000692416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Cys158Tyr
CA402948801
NM_000455.5:c.473G>A