Allele Registry

Canonical Allele Identifier: PA2825940787

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058453

ClinVar Variation:

67689

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Asp596Gly	CA015362 NM_001160160.2:c.1787A>G