Canonical Allele Identifier: PA891851115
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 578100
ClinVar RCV Id: RCV000701013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ala194Val
CA7649457
NM_005477.3:c.581C>T