Canonical Allele Identifier: PA211500
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67391
ClinVar RCV Id: RCV000058113 RCV000148535 RCV000586962 RCV000618893 RCV001162548 RCV001778698 RCV001841708 RCV002228167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Arg791Trp
CA006525
NM_000238.4:c.2371C>T