Canonical Allele Identifier: PA2827769052
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68528
ClinVar RCV Id: RCV000059400 RCV000188829 RCV000550639 RCV001197275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Arg101Gln
CA273119
NM_001353951.2:c.302G>A