Allele Registry

Canonical Allele Identifier: PA302193

Gene: SCN1B HGNC NCBI

ClinVar RCV:

RCV000171060

RCV001350746

RCV002426813

RCV002485076

ClinVar Variation:

190880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028.1:p.Thr28Ala	CA302192 NM_001037.5:c.82A>G