Canonical Allele Identifier: PA166608
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141851
ClinVar RCV Id: RCV000130534 RCV000217158 RCV000527203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala347Gly
CA022211
NM_000455.5:c.1040C>G