Canonical Allele Identifier: PA645449018
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2767097
ClinVar RCV Id: RCV003590451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Phe210Leu
CA385223669
NM_014191.4:c.628T>C
CA385223693
NM_014191.4:c.630T>A
CA385223695
NM_014191.4:c.630T>G