Allele Registry

Canonical Allele Identifier: PA2825537858

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003656750

ClinVar Variation:

966968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Gln419Glu	CA352148654 NM_001099404.2:c.1255C>G