Canonical Allele Identifier: PA2827292922
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1317485
ClinVar RCV Id: RCV001768051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Thr1951Ser
CA384889926
NM_001330260.2:c.5851A>T
CA384889934
NM_001330260.2:c.5852C>G