Canonical Allele Identifier: PA093557
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 253288
ClinVar RCV Id: RCV000239751 RCV000493549 RCV002519872 RCV003335289 RCV003992247
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1327Val
CA10586295
NM_014191.4:c.3979A>G