Canonical Allele Identifier: PA2826011859
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189872
ClinVar RCV Id: RCV000180825 RCV003326125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Pro358Ser
CA303166
NM_001165964.3:c.1072C>T