Allele Registry

Canonical Allele Identifier: PA2825492267

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058711

ClinVar Variation:

67928

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092875.1:p.Glu161Gln	CA018595 NM_001099405.2:c.481G>C