Allele Registry

Canonical Allele Identifier: PA265688

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058711

ClinVar Variation:

67928

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Glu161Gln	CA018595 NM_000335.5:c.481G>C