Canonical Allele Identifier: PA122771
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 12878
ClinVar RCV Id: RCV000013738 RCV000189121 RCV000527590 RCV003224096
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Val892Ile
CA122770
NM_021007.3:c.2674G>A