Allele Registry

Canonical Allele Identifier: PA211821

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058693

RCV000148850

RCV000183081

RCV000987201

RCV001725963

RCV001842367

RCV002336211

ClinVar Variation:

67912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Val1532Ile	CA018450 NM_001099404.2:c.4594G>A