Canonical Allele Identifier: PA2826129918
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2909830
ClinVar RCV Id: RCV003753702
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Thr729Ser
CA236311203
NM_001177984.2:c.2186C>G
CA384879806
NM_001177984.2:c.2185A>T