Canonical Allele Identifier: PA658670391
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 485009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Asp277His
CA402950659
NM_000455.5:c.829G>C