Allele Registry

Canonical Allele Identifier: PA265642

Gene: SCN5A HGNC NCBI

ClinVar Variation Id: 67914

ClinVar RCV Id: RCV000058695

ClinVar Variation Id: 2702720

ClinVar RCV Id: RCV003577512

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Ser1552Arg	CA018469 NM_000335.5:c.4654A>C CA352143902 NM_000335.5:c.4656T>G CA352143903 NM_000335.5:c.4656T>A