Allele Registry

Canonical Allele Identifier: PA2825131788

Gene: SCN5A HGNC NCBI

ClinVar Variation Id: 830371

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Phe1570Leu	CA352143783 NM_000335.5:c.4710C>G CA352143784 NM_000335.5:c.4710C>A CA352143788 NM_000335.5:c.4708T>C