Allele Registry

Canonical Allele Identifier: PA2499241817

Gene: HCN2 HGNC NCBI

ClinVar RCV:

RCV001637971

ClinVar Variation:

1240010

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185.3:p.Ser126Leu	CA402868880 NM_001194.4:c.377C>T