ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826275097
Gene: KCNH2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000057993
RCV000168208
RCV000414552
ClinVar Variation:
67277
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001191727.1:p.Tyr257Cys
CA005509
NM_001204798.2:c.770A>G