Canonical Allele Identifier: PA2827780000
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_001340884.1:p.Tyr1264Phe
CA349054146
NM_001353955.2:c.3791A>T