Canonical Allele Identifier: PA2828475549
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1016869
ClinVar RCV Id: RCV001315940
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asp1246Glu
CA349027817
NM_001371247.1:c.3738C>A
CA349027828
NM_001371247.1:c.3738C>G