Canonical Allele Identifier: PA2741942443
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2817438
ClinVar RCV Id: RCV003754246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Met524Ile
CA385229104
NM_014191.4:c.1572G>A
CA385229105
NM_014191.4:c.1572G>T
CA385229106
NM_014191.4:c.1572G>C