Allele Registry

Canonical Allele Identifier: PA145071

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058426

RCV000144029

RCV000588264

RCV002498340

RCV003996525

ClinVar Variation:

67665

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Thr512Ile	CA014930 NM_001099404.2:c.1535C>T