Canonical Allele Identifier: PA2499271130
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021059
ClinVar RCV Id: RCV001320749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro1062Ser
CA393086055
NM_005477.3:c.3184C>T