Canonical Allele Identifier: PA658670579
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 486517
ClinVar RCV Id: RCV000574766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Lys388Glu
CA402953447
NM_000455.5:c.1162A>G