Canonical Allele Identifier: PA2827787828
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1098587
ClinVar RCV Id: RCV001420525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Val422Leu
CA349070860
NM_001353960.2:c.1264G>T
CA349070861
NM_001353960.2:c.1264G>C