Canonical Allele Identifier: PA1139712796
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 849884
ClinVar RCV Id: RCV001053934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro1164Ala
CA7648815
NM_005477.3:c.3490C>G