Canonical Allele Identifier: PA204239
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Tyr611Asp
CA005628
NM_000238.4:c.1831T>G