Canonical Allele Identifier: PA317774
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206933
ClinVar RCV Id: RCV000189077 RCV001255357 RCV001857651 RCV001253376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly329Cys
CA317771
NM_006920.6:c.985G>T