Allele Registry

Canonical Allele Identifier: PA107886

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058673

ClinVar Variation:

67893

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Gly1481Glu	CA018265 NM_198056.3:c.4442G>A