Allele Registry

Canonical Allele Identifier: PA2825940981

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000458183

ClinVar Variation:

403732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Leu729del	CA16609849 NM_001160160.2:c.2184_2186del