Canonical Allele Identifier: PA302174
Gene: SCN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 190869
ClinVar RCV Id: RCV000171049 RCV000299875 RCV000254455 RCV000588361 RCV001080647 RCV004539576
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028.1:p.Gly10Ser
CA302173
NM_001037.5:c.28G>A