Allele Registry

Canonical Allele Identifier: PA108166

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058601

RCV003996538

ClinVar Variation:

67826

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Lys126Glu	CA017507 NM_198056.3:c.376A>G