Canonical Allele Identifier: PA204238
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67290
ClinVar RCV Id: RCV000058007 RCV000190215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742054.1:p.Tyr271Asp
CA005628
NM_172057.3:c.811T>G