Canonical Allele Identifier: PA645459872
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 236193
ClinVar RCV Id: RCV000225068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp237Tyr
CA10581557
NM_000455.5:c.709G>T