Canonical Allele Identifier: PA301963
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 190781
ClinVar RCV Id: RCV000170940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Cys449Ser
CA301962
NM_005477.3:c.1346G>C
CA393094290
NM_005477.3:c.1345T>A