Canonical Allele Identifier: PA2827790486
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3067157
ClinVar RCV Id: RCV003992846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Met453Ile
CA349054289
NM_001353961.2:c.1359G>T
CA349054291
NM_001353961.2:c.1359G>C
CA349054293
NM_001353961.2:c.1359G>A