Allele Registry

Canonical Allele Identifier: PA2827292525

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000851494

RCV001858503

ClinVar Variation:

691254

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Ile1631Thr	CA384880453 NM_001330260.2:c.4892T>C