Canonical Allele Identifier: PA328958
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67299
ClinVar RCV Id: RCV000058017 RCV001208803 RCV000845307 RCV001781395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Ser621Asn
CA005703
NM_000238.4:c.1862G>A