Canonical Allele Identifier: PA2825352769
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 864391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Glu130Lys
CA405328925
NM_001037.5:c.388G>A