Canonical Allele Identifier: PA2825144029
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2124990
ClinVar RCV Id: RCV003039893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000446.1:p.Thr230Ser
CA402949802
NM_000455.5:c.688A>T
CA402949806
NM_000455.5:c.689C>G