Canonical Allele Identifier: PA645459990
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 418883
ClinVar RCV Id: RCV000482762 RCV001010118 RCV001809431
ClinVar Variation Id: 2679056
ClinVar RCV Id: RCV003466419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Val390Leu
CA16620758
NM_000455.5:c.1168G>C
CA402953489
NM_000455.5:c.1168G>T