Canonical Allele Identifier: PA144951
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67162
ClinVar RCV Id: RCV000057869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000229.1:p.Asp342Val
CA004177
NM_000238.4:c.1025A>T