Canonical Allele Identifier: PA2580442265
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2417887
ClinVar RCV Id: RCV003117996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ala215Val
CA1939669
NM_021007.3:c.644C>T