Canonical Allele Identifier: PA1139725798
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 842452
ClinVar RCV Id: RCV001044878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Gln1478Glu
CA349034330
NM_021007.3:c.4432C>G