Canonical Allele Identifier: PA234847
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_008851.3:p.Lys1259Asn
CA234845
NM_006920.6:c.3777A>C
CA349054259
NM_006920.6:c.3777A>T