Canonical Allele Identifier: PA2827786016
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 571695
ClinVar RCV Id: RCV000692909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Phe1302Ser
CA349052909
NM_001353958.2:c.3905T>C