Allele Registry

Canonical Allele Identifier: PA145117

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058714

RCV003541167

RCV004019055

ClinVar Variation:

67931

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Thr1619Lys	CA018648 NM_000335.5:c.4856C>A