Canonical Allele Identifier: PA187610
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 184047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ala420Val
CA022562
NM_000455.5:c.1259C>T