Canonical Allele Identifier: PA1139712496
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 948442
ClinVar RCV Id: RCV001219696
ClinVar Variation Id: 2746152
ClinVar RCV Id: RCV003504655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Gly885Arg
CA7648979
NM_005477.3:c.2653G>A
CA393088476
NM_005477.3:c.2653G>C