Canonical Allele Identifier: PA2826013055
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167638
ClinVar RCV Id: RCV000153887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Lys1242Asn
CA234845
NM_001165964.3:c.3726A>C
CA349054259
NM_001165964.3:c.3726A>T