Allele Registry

Canonical Allele Identifier: PA2825940758

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058449

ClinVar Variation:

67685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Gln573Glu	CA015285 NM_001160160.2:c.1717C>G