Allele Registry

Canonical Allele Identifier: PA092629

Gene: KCNH2 HGNC NCBI

ClinVar RCV:

RCV000057961

ClinVar Variation:

67249

HGVS (amino-acid)	Matching Registered Transcripts
NP_000229.1:p.Gly572Cys	CA005257 NM_000238.4:c.1714G>T