Canonical Allele Identifier: PA144961
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67297
ClinVar RCV Id: RCV000058015 RCV001376739 RCV002408565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Thr618Ile
CA005690
NM_000238.4:c.1853C>T