Allele Registry

Canonical Allele Identifier: PA2827922020

Gene: SCN5A HGNC NCBI

ClinVar Allele:

393587

ClinVar RCV:

RCV000463581

RCV001841356

ClinVar Variation:

406436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Lys590Gln	CA16611286 NM_001354701.2:c.1768A>C