Canonical Allele Identifier: PA2829676150
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1067239
ClinVar RCV Id: RCV001378447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ile1534Lys
CA349072268
NM_006920.6:c.4601T>A