Canonical Allele Identifier: PA2827783019
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2002938
ClinVar RCV Id: RCV002833103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Leu1281Pro
CA349053255
NM_001353957.2:c.3842T>C