Canonical Allele Identifier: PA285059
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68584
ClinVar RCV Id: RCV000059460 RCV000808399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg322Ile
CA285057
NM_006920.6:c.965G>T