Canonical Allele Identifier: PA166894
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141954
ClinVar RCV Id: RCV000130688 RCV000230363 RCV001800436 RCV002478395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr395Ala
CA022417
NM_000455.5:c.1183A>G