Allele Registry

Canonical Allele Identifier: PA2825942068

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058660

ClinVar Variation:

67880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153632.1:p.Pro1437Leu	CA018135 NM_001160160.2:c.4310C>T