Canonical Allele Identifier: PA300019
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 182906
ClinVar RCV Id: RCV000161000 RCV000411610 RCV000575310 RCV000761133 RCV000781888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Val133Met
CA022888
NM_000455.5:c.397G>A