Canonical Allele Identifier: PA211499
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742054.1:p.Arg451Trp
CA006525
NM_172057.3:c.1351C>T