Allele Registry

Canonical Allele Identifier: PA2827921480

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV000182935

ClinVar Variation:

201436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341630.1:p.Ala204Glu	CA019632 NM_001354701.2:c.611C>A