Canonical Allele Identifier: PA2826275024
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67243
ClinVar Variation Id: 67244
ClinVar RCV Id: RCV000057955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Trp228Cys
CA005198
NM_001204798.2:c.684G>C
CA005206
NM_001204798.2:c.684G>T