Canonical Allele Identifier: PA2826275100
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Ser259Arg
CA005518
NM_001204798.2:c.777C>A
CA369858048
NM_001204798.2:c.777C>G
CA369858054
NM_001204798.2:c.775A>C