Canonical Allele Identifier: PA2828475445
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3026693
ClinVar RCV Id: RCV003887086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Lys1178Met
CA349025769
NM_001371247.1:c.3533A>T