Canonical Allele Identifier: PA645459972
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 234671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Pro373Leu
CA10577599
NM_000455.5:c.1118C>T