Canonical Allele Identifier: PA2825353546
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2417887
ClinVar RCV Id: RCV003117996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ala215Val
CA1939669
NM_001040142.2:c.644C>T