Canonical Allele Identifier: PA891855355
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 573377
ClinVar RCV Id: RCV000695035 RCV001565909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Met1600Ile
CA384880261
NM_014191.4:c.4800G>A
CA384880262
NM_014191.4:c.4800G>C
CA384880263
NM_014191.4:c.4800G>T