Allele Registry

Canonical Allele Identifier: PA094633

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV000128815

ClinVar Variation:

140599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035241.1:p.Arg6Lys	CA163443 NM_001040151.2:c.17G>A