Canonical Allele Identifier: PA2573170764
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1498658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Ser325Thr
CA402951589
NM_000455.5:c.974G>C