Allele Registry

Canonical Allele Identifier: PA2825129453

Gene: SCN5A HGNC NCBI

ClinVar Allele:

1296638

ClinVar RCV:

RCV001770875

ClinVar Variation:

1306695

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Val563Leu	CA352146717 NM_000335.5:c.1687G>T CA352146720 NM_000335.5:c.1687G>C