Canonical Allele Identifier: PA2827782996
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 836073
ClinVar RCV Id: RCV001037109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Val1266Phe
CA349053549
NM_001353957.2:c.3796G>T