Canonical Allele Identifier: PA2827788074
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1186442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ser642Asn
CA1943230
NM_001353960.2:c.1925G>A