Canonical Allele Identifier: PA2827782142
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1186442
ClinVar RCV Id: RCV001545535 RCV002568276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ser643Asn
CA1943230
NM_001353957.2:c.1928G>A