Canonical Allele Identifier: PA658670228
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 485022
ClinVar RCV Id: RCV000567764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Met127Ile
CA402948100
NM_000455.5:c.381G>A
CA402948101
NM_000455.5:c.381G>C
CA402948103
NM_000455.5:c.381G>T