Canonical Allele Identifier: PA2827069501
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 60768
ClinVar RCV Id: RCV000054538 RCV000171064 RCV000234993 RCV000766769 RCV000620098 RCV001853079 RCV002477176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308534.1:p.Asp120Asn
CA144662
NM_001321605.1:c.358G>A