Allele Registry

Canonical Allele Identifier: PA2827921730

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058402

ClinVar Variation:

67645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Gly400Ala	CA014496 NM_001354701.2:c.1199G>C