Canonical Allele Identifier: PA329494
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67489
ClinVar RCV Id: RCV000058218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Asp111Val
CA008196
NM_000238.4:c.332A>T