Canonical Allele Identifier: PA2741920257
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747170
ClinVar RCV Id: RCV003504677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ser164Trp
CA393097858
NM_005477.3:c.491C>G