Allele Registry

Canonical Allele Identifier: PA2826275038

Gene: KCNH2 HGNC NCBI

ClinVar RCV:

RCV000057961

ClinVar Variation:

67249

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191727.1:p.Gly232Cys	CA005257 NM_001204798.2:c.694G>T