Canonical Allele Identifier: PA166612
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141852
ClinVar RCV Id: RCV000130536 RCV000705839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro413Leu
CA022521
NM_000455.5:c.1238C>T