Canonical Allele Identifier: PA645459971
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403782
ClinVar RCV Id: RCV000474669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Gln371Leu
CA16616034
NM_000455.5:c.1112A>T