Allele Registry

Canonical Allele Identifier: PA2825494037

Gene: SCN5A HGNC NCBI

ClinVar Variation Id: 201469

ClinVar RCV Id: RCV000182995

ClinVar Variation Id: 1906128

ClinVar RCV Id: RCV003776596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092875.1:p.Cys683Ser	CA015794 NM_001099405.2:c.2048G>C CA352144892 NM_001099405.2:c.2047T>A