Canonical Allele Identifier: PA2827785332
Gene: SCN1A HGNC NCBI
ClinVar RCV:
RCV000180911
ClinVar Variation:
189957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Glu818Gly
CA303403
NM_001353958.2:c.2453A>G