Allele Registry

Canonical Allele Identifier: PA308041

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV002074453

ClinVar Variation:

1527869

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Arg893Leu	CA016400 NM_198056.3:c.2678G>T