Allele Registry

Canonical Allele Identifier: PA2827922234

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV001842185

ClinVar Variation:

1332147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Ala735Gly	CA352144545 NM_001354701.2:c.2204C>G