Allele Registry

Canonical Allele Identifier: PA144962

Gene: KCNH2 HGNC NCBI

ClinVar Variation Id: 67297

HGVS (amino-acid)	Matching Registered Transcripts
NP_742053.1:p.Thr618Ile	CA005690 NM_172056.2:c.1853C>T