Canonical Allele Identifier: PA2573170698
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ser307Arg
CA402951337
NM_000455.5:c.919A>C
CA402951417
NM_000455.5:c.921C>A
CA402951418
NM_000455.5:c.921C>G