Canonical Allele Identifier: PA2826014195
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.His1901Gln
CA16610265
NM_001165964.3:c.5703C>G
CA349063878
NM_001165964.3:c.5703C>A