Canonical Allele Identifier: PA645407753
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 372556
ClinVar RCV Id: RCV000414308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ser1621Pro
CA16042357
NM_021007.3:c.4861T>C