Canonical Allele Identifier: PA2826259909
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 986202
ClinVar RCV Id: RCV001267495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Asn1417Ile
CA349049929
NM_001202435.3:c.4250A>T