Canonical Allele Identifier: PA2573205440
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1505698
ClinVar RCV Id: RCV001999575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ser484Thr
CA349053473
NM_001353961.2:c.1451G>C