Canonical Allele Identifier: PA2827069609
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 190874
ClinVar RCV Id: RCV000171054 RCV000646745 RCV002354422 RCV002478539 RCV004535162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308534.1:p.Ala164Val
CA302180
NM_001321605.1:c.491C>T