Canonical Allele Identifier: PA915997702
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 666148
ClinVar RCV Id: RCV000824582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Asp491His
CA393093803
NM_005477.3:c.1471G>C