Canonical Allele Identifier: PA2827768699
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450597
ClinVar RCV Id: RCV000523148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Glu1960Gln
CA349063242
NM_001353950.2:c.5878G>C