Canonical Allele Identifier: PA645498946
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 374861
ClinVar RCV Id: RCV000415571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ala414Gly
CA16043944
NM_005477.3:c.1241C>G