Allele Registry

Canonical Allele Identifier: PA265073

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058496

RCV002223183

ClinVar Variation:

67727

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Pro773Ser	CA016076 NM_001099404.2:c.2317C>T