Canonical Allele Identifier: PA2827777140
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12885
ClinVar RCV Id: RCV000013745 RCV000059409 RCV003992150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Val1341Leu
CA256593
NM_001353954.2:c.4021G>C