Canonical Allele Identifier: PA300030
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 182914
ClinVar RCV Id: RCV000161009 RCV000470806 RCV000579540 RCV003467272
ClinVar Variation Id: 819421
ClinVar RCV Id: RCV001011961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Met51Leu
CA022670
NM_000455.5:c.151A>C
CA402944074
NM_000455.5:c.151A>T