Canonical Allele Identifier: PA2826258597
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1675810
ClinVar RCV Id: RCV002214179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Met447Ile
CA349070396
NM_001202435.3:c.1341G>T
CA349070399
NM_001202435.3:c.1341G>A
CA349070402
NM_001202435.3:c.1341G>C