Allele Registry

Canonical Allele Identifier: PA144961

Gene: KCNH2 HGNC NCBI

ClinVar RCV:

RCV000058015

RCV001376739

RCV002408565

ClinVar Variation:

67297

HGVS (amino-acid)	Matching Registered Transcripts
NP_000229.1:p.Thr618Ile	CA005690 NM_000238.4:c.1853C>T