Canonical Allele Identifier: PA2827779035
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1189857
ClinVar RCV Id: RCV001550380 RCV002568316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Lys546Asn
CA1943282
NM_001353955.2:c.1638G>T
CA349069050
NM_001353955.2:c.1638G>C