Canonical Allele Identifier: PA891862000
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_001159435.1:p.Phe1330Ser
CA349052909
NM_001165963.4:c.3989T>C