Allele Registry

Canonical Allele Identifier: PA2826275000

Gene: KCNH2 HGNC NCBI

ClinVar RCV:

RCV000434772

ClinVar Variation:

379052

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191727.1:p.His222Gln	CA16605170 NM_001204798.2:c.666C>G CA369858791 NM_001204798.2:c.666C>A