Allele Registry

Canonical Allele Identifier: PA2827921761

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003656750

ClinVar Variation:

966968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Gln419Glu	CA352148654 NM_001354701.2:c.1255C>G