Allele Registry

Canonical Allele Identifier: PA264883

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058391

RCV004017376

ClinVar Variation:

67634

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Arg367Leu	CA014324 NM_198056.3:c.1100G>T