Allele Registry

Canonical Allele Identifier: PA2825130264

Gene: SCN5A HGNC NCBI

ClinVar RCV:

RCV003772766

ClinVar Variation:

1403991

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Ser941Ile	CA2573136282 NM_000335.5:c.2821_2822delinsAT