Allele Registry

Canonical Allele Identifier: PA265799

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058750

RCV003542279

ClinVar Variation:

67964

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092874.1:p.Cys1728Trp	CA018961 NM_001099404.2:c.5184C>G