Canonical Allele Identifier: PA329466
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67477
ClinVar RCV Id: RCV000058206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Phe106Tyr
CA008078
NM_000238.4:c.317T>A