Allele Registry

Canonical Allele Identifier: PA211856

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058503

RCV000148860

RCV000239085

RCV000987215

RCV001842315

RCV002426618

ClinVar Variation:

67734

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Gly833Arg	CA016206 NM_198056.3:c.2497G>A CA352142529 NM_198056.3:c.2497G>C