Canonical Allele Identifier: PA317616
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206867
ClinVar RCV Id: RCV000189005 RCV000714534 RCV000714535 RCV003128153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1834Val
CA317613
NM_001165963.4:c.5501C>T