Allele Registry

Canonical Allele Identifier: PA265798

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058750

RCV003542279

ClinVar Variation:

67964

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Cys1727Trp	CA018961 NM_000335.5:c.5181C>G