Allele Registry

Canonical Allele Identifier: PA2825361285

Gene: SCN3B HGNC NCBI

ClinVar RCV:

RCV001842965

RCV002515579

ClinVar Variation:

224720

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035241.1:p.Ile141Met	CA10575989 NM_001040151.2:c.423C>G