Canonical Allele Identifier: PA2827771282
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2833642
ClinVar RCV Id: RCV003754473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Gly1408Arg
CA349049919
NM_001353951.2:c.4222G>C
CA349049920
NM_001353951.2:c.4222G>A