Allele Registry

Canonical Allele Identifier: PA2825942266

Gene: SCN5A HGNC NCBI

ClinVar Variation Id: 830371

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Phe1570Leu	CA352143783 NM_001160160.2:c.4710C>G CA352143784 NM_001160160.2:c.4710C>A CA352143788 NM_001160160.2:c.4708T>C