Canonical Allele Identifier: PA2826011700
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2664199
ClinVar RCV Id: RCV003445334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly265Arg
CA349073348
NM_001165964.3:c.793G>C
CA349073350
NM_001165964.3:c.793G>A