Canonical Allele Identifier: PA2826259341
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 425226
ClinVar RCV Id: RCV000487912 RCV001448434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Tyr1025Phe
CA1943013
NM_001202435.3:c.3074A>T