Allele Registry

Canonical Allele Identifier: PA094643

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV000128814

ClinVar Variation:

140598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035241.1:p.Met161Thr	CA163440 NM_001040151.2:c.482T>C