Allele Registry

Canonical Allele Identifier: PA2827921974

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV001254773

RCV004004921

ClinVar Variation:

977183

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.His558Tyr	CA72939207 NM_001354701.2:c.1672C>T