Allele Registry

Canonical Allele Identifier: PA2825942139

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058673

ClinVar Variation:

67893

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Gly1480Glu	CA018265 NM_001160160.2:c.4439G>A