Canonical Allele Identifier: PA2827781849
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2572473
ClinVar RCV Id: RCV003314358 RCV003753267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Gly396Arg
CA349071024
NM_001353957.2:c.1186G>C
CA349071025
NM_001353957.2:c.1186G>A