Canonical Allele Identifier: PA915966431
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 818617
ClinVar RCV Id: RCV001010375 RCV001050408 RCV002465820 RCV003467590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala406Gly
CA402953796
NM_000455.5:c.1217C>G