Allele Registry

Canonical Allele Identifier: PA2825944773

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000183046

ClinVar Variation:

201500

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153633.1:p.Asp1221Tyr	CA017536 NM_001160161.2:c.3661G>T