Canonical Allele Identifier: PA2573245685
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480609
ClinVar RCV Id: RCV002000332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro842Ser
CA393088730
NM_005477.3:c.2524C>T