Canonical Allele Identifier: PA2826274802
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67183
ClinVar Variation Id: 519399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Phe91Leu
CA004434
NM_001204798.2:c.273C>A
CA369860049
NM_001204798.2:c.273C>G
CA369860054
NM_001204798.2:c.271T>C