Allele Registry

Canonical Allele Identifier: PA107663

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058776

RCV003542282

ClinVar Variation:

67989

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Asp1790Gly	CA019174 NM_198056.3:c.5369A>G