Canonical Allele Identifier: PA2827769007
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 958033
ClinVar RCV Id: RCV001231119 RCV002451545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Asn86Ser
CA60270523
NM_001353951.2:c.257A>G