Allele Registry

Canonical Allele Identifier: PA307651

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058667

RCV000183071

ClinVar Variation:

67887

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Ser1457Tyr	CA018188 NM_000335.5:c.4370C>A