Allele Registry

Canonical Allele Identifier: PA307571

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000183046

ClinVar Variation:

201500

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Asp1275Tyr	CA017536 NM_198056.3:c.3823G>T