Canonical Allele Identifier: PA2573089201
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309236
ClinVar RCV Id: RCV001765405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Val1329Gly
CA349026038
NM_006922.4:c.3986T>G