Canonical Allele Identifier: PA304813
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67321
ClinVar RCV Id: RCV000058040 RCV000181824 RCV000621397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742054.1:p.Pro292Ser
CA005893
NM_172057.3:c.874C>T