Canonical Allele Identifier: PA2827788201
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189917
ClinVar RCV Id: RCV000180869 RCV001071061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Met756Val
CA303300
NM_001353960.2:c.2266A>G