Canonical Allele Identifier: PA1139740890
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_001340890.1:p.Val480Phe
CA349053549
NM_001353961.2:c.1438G>T