Allele Registry

Canonical Allele Identifier: PA645504660

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000458183

ClinVar Variation:

403732

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Leu729del	CA16609849 NM_198056.3:c.2184_2186del