Canonical Allele Identifier: PA2573062780
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332663
ClinVar RCV Id: RCV001805709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr189Ala
CA402949203
NM_000455.5:c.565A>G