Canonical Allele Identifier: PA658808666
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 538088
ClinVar RCV Id: RCV000647245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ile793Leu
CA393089010
NM_005477.3:c.2377A>T
CA393089012
NM_005477.3:c.2377A>C