Canonical Allele Identifier: PA318209
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Leu216Trp
CA318208
NM_001040142.2:c.647T>G