Canonical Allele Identifier: PA2741974387
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3026693
ClinVar RCV Id: RCV003887086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Lys1178Met
CA349025769
NM_021007.3:c.3533A>T