Canonical Allele Identifier: PA2829675779
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1505698
ClinVar RCV Id: RCV001999575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ser1287Thr
CA349053473
NM_006920.6:c.3860G>C