Canonical Allele Identifier: PA328513
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67193
ClinVar RCV Id: RCV000057900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742053.1:p.Phe463Leu
CA004552
NM_172056.2:c.1387T>C
CA369859853
NM_172056.2:c.1389C>G
CA369859854
NM_172056.2:c.1389C>A