Canonical Allele Identifier: PA167799
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 142223
ClinVar RCV Id: RCV000131221 RCV000541150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Met18Leu
CA023063
NM_000455.5:c.52A>C
CA402943322
NM_000455.5:c.52A>T