Canonical Allele Identifier: PA1139712449
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 936716
ClinVar RCV Id: RCV001205571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Phe857Leu
CA7648998
NM_005477.3:c.2571C>G
CA393088636
NM_005477.3:c.2571C>A
CA393088641
NM_005477.3:c.2569T>C