Allele Registry

Canonical Allele Identifier: PA2825942535

Gene: SCN5A HGNC NCBI

ClinVar Allele:

78872

ClinVar RCV:

RCV000058766

RCV000183198

RCV000620629

RCV000660252

ClinVar Variation:

67980

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Ile1735Val	CA019094 NM_001160160.2:c.5203A>G