Canonical Allele Identifier: PA2825099169
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 660517
ClinVar Variation Id: 1790023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Arg784Pro
CA369856062
NM_000238.4:c.2351G>C
CA915945573
NM_000238.4:c.2351_2352delinsCC