Canonical Allele Identifier: PA168251
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142404
ClinVar RCV Id: RCV000131503 RCV000229523 RCV000486911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ser422del
CA022566
NM_000455.5:c.1265_1267del