Canonical Allele Identifier: PA2828475157
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1995460
ClinVar RCV Id: RCV002796600
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asp997Asn
CA349019576
NM_001371247.1:c.2989G>A