Canonical Allele Identifier: PA2826259177
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189978
ClinVar RCV Id: RCV000180933 RCV004535159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Cys927Phe
CA303467
NM_001202435.3:c.2780G>T