Canonical Allele Identifier: PA2825479678
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 1036370
ClinVar RCV Id: RCV001339373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Val1280Ile
CA1938660
NM_001081676.2:c.3838G>A