Canonical Allele Identifier: PA317652
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206876
ClinVar RCV Id: RCV000189015 RCV000986869 RCV001071764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1894Thr
CA317649
NM_001165963.4:c.5681T>C