Canonical Allele Identifier: PA287491
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 127699
ClinVar RCV Id: RCV000115595 RCV000195603 RCV000576049 RCV001798331 RCV003235043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala397Ser
CA022429
NM_000455.5:c.1189G>T