Canonical Allele Identifier: PA188572
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184313
ClinVar RCV Id: RCV000163543 RCV000204629 RCV001539393 RCV003387780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg211Trp
CA023186
NM_000455.5:c.631C>T