Canonical Allele Identifier: PA328949
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67296
ClinVar RCV Id: RCV000058014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742053.1:p.Thr618Ser
CA005683
NM_172056.2:c.1853C>G
CA369857951
NM_172056.2:c.1852A>T