Canonical Allele Identifier: PA2741942950
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2828198
ClinVar RCV Id: RCV003754390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Met1645Ile
CA384880581
NM_014191.4:c.4935G>A
CA384880583
NM_014191.4:c.4935G>C
CA384880584
NM_014191.4:c.4935G>T