Canonical Allele Identifier: PA2826258261
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68672
ClinVar RCV Id: RCV000059552 RCV001569540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ile252Asn
CA285255
NM_001202435.3:c.755T>A