Canonical Allele Identifier: PA189731
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184692
ClinVar RCV Id: RCV000163989 RCV000217261 RCV000553557 RCV000766875 RCV001358183 RCV003467283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro326Thr
CA023391
NM_000455.5:c.976C>A