Canonical Allele Identifier: PA304819
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67323
ClinVar RCV Id: RCV000058042 RCV000181825 RCV000678919 RCV000617489 RCV000799027 RCV004549483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742053.1:p.Asn633Ser
CA005905
NM_172056.2:c.1898A>G