Allele Registry

Canonical Allele Identifier: PA265610

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058684

RCV000709759

RCV000756618

RCV001201272

RCV001842366

RCV003162459

RCV004537262

ClinVar Variation:

67904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Leu1501Val	CA018357 NM_001099404.2:c.4501C>G