Canonical Allele Identifier: PA2825352565
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 852686
ClinVar RCV Id: RCV001057345 RCV002451237 RCV002479349
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Glu84Lys
CA405328608
NM_001037.5:c.250G>A