Allele Registry

Canonical Allele Identifier: PA163439

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV000128813

RCV000480040

RCV001320720

ClinVar Variation:

140597

HGVS (amino-acid)	Matching Registered Transcripts
NP_060870.1:p.Ala130Val	CA163437 NM_018400.3:c.389C>T