Canonical Allele Identifier: PA645376177
Gene: HCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 252561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185.3:p.Pro719_Pro721del
CA9018841
NM_001194.4:c.2156_2164del