Canonical Allele Identifier: PA2573256301
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1407277
ClinVar RCV Id: RCV001918359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Thr1888Ser
CA6571937
NM_014191.4:c.5662A>T
CA384888392
NM_014191.4:c.5663C>G