Canonical Allele Identifier: PA2826274941
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67218
ClinVar RCV Id: RCV000057927 RCV000698598 RCV001664237 RCV001269138 RCV002470743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191727.1:p.Arg191Trp
CA004871
NM_001204798.2:c.571C>T