Canonical Allele Identifier: PA162201
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 7461
ClinVar RCV Id: RCV000007887 RCV000115593 RCV000122091 RCV000656543 RCV001355263 RCV001797996 RCV002504766
ClinVar Variation Id: 376711
ClinVar RCV Id: RCV000419471 RCV001397182 RCV002411286
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Phe354Leu
CA022247
NM_000455.5:c.1062C>G
CA16603121
NM_000455.5:c.1060T>C
CA402951852
NM_000455.5:c.1062C>A