Canonical Allele Identifier: PA2828475310
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435680
ClinVar RCV Id: RCV003136430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Phe1095Leu
CA349021689
NM_001371247.1:c.3283T>C
CA349021701
NM_001371247.1:c.3285T>G
CA349021703
NM_001371247.1:c.3285T>A