Allele Registry

Canonical Allele Identifier: PA2825941809

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000183046

ClinVar Variation:

201500

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Asp1274Tyr	CA017536 NM_001160160.2:c.3820G>T