Canonical Allele Identifier: PA2827786822
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68569
ClinVar RCV Id: RCV000059444 RCV001854242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Met1752Thr
CA285018
NM_001353958.2:c.5255T>C