Allele Registry

Canonical Allele Identifier: PA2825940686

Gene: SCN5A HGNC NCBI

ClinVar Allele:

78566

ClinVar RCV:

RCV000058434

RCV000182979

RCV000490338

RCV001842287

RCV002483110

ClinVar Variation:

67671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Phe532Cys	CA015051 NM_001160160.2:c.1595T>G