Canonical Allele Identifier: PA2826275139
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Tyr271His
CA005621
NM_001204798.2:c.811T>C