Canonical Allele Identifier: PA2825098650
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043131
ClinVar RCV Id: RCV001347193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Thr337Ser
CA026662
NM_000238.4:c.1010C>G
CA369861659
NM_000238.4:c.1009A>T