Canonical Allele Identifier: PA2741874058
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2630146
ClinVar RCV Id: RCV004527832
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Val211Leu
CA385224421
NM_001369788.1:c.631G>C
CA385224426
NM_001369788.1:c.631G>T