Canonical Allele Identifier: PA645499163
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 392636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro968Leu
CA7648930
NM_005477.3:c.2903C>T