Canonical Allele Identifier: PA2828470838
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 421470
ClinVar RCV Id: RCV000478420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Thr435Ile
CA16617263
NM_001371246.1:c.1304C>T