Allele Registry

Canonical Allele Identifier: PA163445

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV000128815

ClinVar Variation:

140599

HGVS (amino-acid)	Matching Registered Transcripts
NP_060870.1:p.Arg6Lys	CA163443 NM_018400.3:c.17G>A