Allele Registry

Canonical Allele Identifier: PA163442

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV000128814

ClinVar Variation:

140598

HGVS (amino-acid)	Matching Registered Transcripts
NP_060870.1:p.Met161Thr	CA163440 NM_018400.3:c.482T>C