Canonical Allele Identifier: PA658731298
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 492741
ClinVar RCV Id: RCV000581400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp176Ala
CA402949012
NM_000455.5:c.527A>C