Canonical Allele Identifier: PA645460027
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ser421Leu
CA10581019
NM_000455.5:c.1261_1262delinsCT