Allele Registry

Canonical Allele Identifier: PA2827923717

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058746

RCV001753476

ClinVar Variation:

67960

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Asn1703Asp	CA018943 NM_001354701.2:c.5107A>G