Canonical Allele Identifier: PA915966421
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 646005
ClinVar RCV Id: RCV000800204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg384Leu
CA402953387
NM_000455.5:c.1151G>T