Allele Registry

Canonical Allele Identifier: PA2827921311

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058530

ClinVar Variation:

67760

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Ile94Ser	CA016537 NM_001354701.2:c.281T>G