Canonical Allele Identifier: PA092878
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67309
ClinVar RCV Id: RCV000058027 RCV002513755
ClinVar Variation Id: 67310
ClinVar RCV Id: RCV000058028
ClinVar Variation Id: 200747
ClinVar RCV Id: RCV000182034 RCV001385333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Phe627Leu
CA005780
NM_000238.4:c.1879T>C
CA005788
NM_000238.4:c.1881C>A
CA005797
NM_000238.4:c.1881C>G