Canonical Allele Identifier: PA218681
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67439
ClinVar RCV Id: RCV000058165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742054.1:p.Gly585Arg
CA007384
NM_172057.3:c.1753G>A
CA369853430
NM_172057.3:c.1753G>C