Canonical Allele Identifier: PA2826274995
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Ala221Thr
CA005019
NM_001204798.2:c.661G>A