Allele Registry

Canonical Allele Identifier: PA2827475558

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000144935

RCV001808403

RCV002460046

RCV002512564

ClinVar Variation:

157600

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336182.1:p.Ile381Thr	CA171014 NM_001349253.2:c.1142T>C