Allele Registry

Canonical Allele Identifier: PA307505

Gene: SCN5A HGNC NCBI

ClinVar Allele:

78677

ClinVar RCV:

RCV000058554

RCV000183027

RCV000766797

RCV000987211

RCV001842330

RCV002321559

ClinVar Variation:

67782

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Thr1069Met	CA016900 NM_001099404.2:c.3206C>T