Allele Registry

Canonical Allele Identifier: PA211875

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058835

RCV000148865

RCV000182942

RCV000521042

RCV000620248

RCV001842405

RCV002477205

RCV004545872

ClinVar Variation:

68032

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Arg225Trp	CA019714 NM_000335.5:c.673C>T