Canonical Allele Identifier: PA2573239987
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 666404
ClinVar RCV Id: RCV001869261 RCV002434034
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Val99Met
CA6300486
NM_004588.5:c.295G>A