Allele Registry

Canonical Allele Identifier: PA329952

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058548

RCV001553202

ClinVar Variation:

67777

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Arg104Gly	CA016820 NM_198056.3:c.310C>G