Canonical Allele Identifier: PA645459939
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 230490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Arg331Trp
CA10581014
NM_000455.5:c.991C>T