Allele Registry

Canonical Allele Identifier: PA916025091

Gene: SCN1B HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

24291

ClinVar RCV:

RCV000009834

RCV000030434

RCV000171041

RCV000184010

RCV000646741

RCV000763042

RCV002316188

RCV004532319

ClinVar Variation:

9252

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308534.1:p.Cys88Trp	CA203839 NM_001321605.1:c.264C>G