Canonical Allele Identifier: PA916060948
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 647893
ClinVar RCV Id: RCV000802514
ClinVar Variation Id: 1754613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_742053.1:p.His221Gln
CA040187
NM_172056.2:c.663C>A
CA369862914
NM_172056.2:c.663C>G