Canonical Allele Identifier: PA304861
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67352
ClinVar RCV Id: RCV000058072 RCV000181833 RCV000468503 RCV000621327 RCV000851290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742053.1:p.Ser660Leu
CA006139
NM_172056.2:c.1979C>T