Canonical Allele Identifier: PA2827767658
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189897
ClinVar RCV Id: RCV000180849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Asn1661His
CA303241
NM_001353950.2:c.4981A>C