Allele Registry

Canonical Allele Identifier: PA1139761224

Gene: SCN5A HGNC NCBI

ClinVar Variation Id: 919932

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Ser1609Leu	CA063800 NM_198056.3:c.4826C>T