Allele Registry

Canonical Allele Identifier: PA265097

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058505

RCV003556149

ClinVar Variation:

67736

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Asp84Asn	CA016221 NM_198056.3:c.250G>A