Canonical Allele Identifier: PA2826275160
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67296
ClinVar RCV Id: RCV000058014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Thr278Ser
CA005683
NM_001204798.2:c.833C>G
CA369857951
NM_001204798.2:c.832A>T