Canonical Allele Identifier: PA2580564928
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2201709
ClinVar RCV Id: RCV002629799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_950238.1:p.His223Asn
CA9372050
NM_199037.5:c.667C>A