Canonical Allele Identifier: PA300040
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 182919
ClinVar Variation Id: 237793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Cys418Ser
CA022540
NM_000455.5:c.1252T>A
CA10583794
NM_000455.5:c.1253G>C