Canonical Allele Identifier: PA2827771599
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1676352
ClinVar RCV Id: RCV002221734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Val1599Leu
CA349071330
NM_001353951.2:c.4795G>C
CA349071335
NM_001353951.2:c.4795G>T