Canonical Allele Identifier: PA276942
Gene: KCNJ11 HGNC NCBI

Linked Data

ClinVar Variation Id: 211230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000516.3:p.Thr294Met
CA276941
NM_000525.4:c.881C>T