Canonical Allele Identifier: PA2827771039
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 852276
ClinVar RCV Id: RCV001056848 RCV003259069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Tyr1265Phe
CA349054146
NM_001353951.2:c.3794A>T