Canonical Allele Identifier: PA2825479680
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2702207
ClinVar RCV Id: RCV003577251

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Val1280Ala
CA349026044
NM_001081676.2:c.3839T>C