Allele Registry

Canonical Allele Identifier: PA2825940165

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058711

ClinVar Variation:

67928

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Glu161Gln	CA018595 NM_001160160.2:c.481G>C