Allele Registry

Canonical Allele Identifier: PA265904

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000058829

RCV003541454

ClinVar Variation:

68029

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Leu212Gln	CA019670 NM_000335.5:c.635T>A