Canonical Allele Identifier: PA658803278
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 527820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp207Gly
CA402949472
NM_000455.5:c.620A>G