Canonical Allele Identifier: PA304761
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67251
ClinVar RCV Id: RCV000057963 RCV000181812 RCV003531953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742053.1:p.Gly572Val
CA005271
NM_172056.2:c.1715G>T