Canonical Allele Identifier: PA332169
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 135277
ClinVar RCV Id: RCV000122092 RCV000206210 RCV000219976 RCV000656983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr363Ile
CA022281
NM_000455.5:c.1088C>T