Canonical Allele Identifier: PA2827775156
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.His1918Gln
CA16610265
NM_001353952.2:c.5754C>G
CA349063878
NM_001353952.2:c.5754C>A