Canonical Allele Identifier: PA266131
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68664
ClinVar RCV Id: RCV000059544 RCV000180879 RCV001854247
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Met1841Thr
CA266129
NM_006920.6:c.5522T>C