Canonical Allele Identifier: PA164237
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 141018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ile35Val
CA022205
NM_000455.5:c.103A>G