Canonical Allele Identifier: PA2828361398
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 664289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Leu1607Phe
CA384880625
NM_001369788.1:c.4821G>C
CA384880628
NM_001369788.1:c.4821G>T