Canonical Allele Identifier: PA166705
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141886
ClinVar RCV Id: RCV000130584 RCV000206247 RCV000482308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Gly346Ser
CA022187
NM_000455.5:c.1036G>A