Canonical Allele Identifier: PA2573090471
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1317485
ClinVar RCV Id: RCV001768051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Thr1951Ser
CA384889926
NM_014191.4:c.5851A>T
CA384889934
NM_014191.4:c.5852C>G