Canonical Allele Identifier: PA2827782635
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 194617
ClinVar RCV Id: RCV000462390 RCV000585632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.His992Gln
CA240694
NM_001353957.2:c.2976C>A
CA349060180
NM_001353957.2:c.2976C>G