Canonical Allele Identifier: PA1139714459
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 916181
ClinVar RCV Id: RCV001171719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ala104del
CA1139655708
NM_006920.6:c.310_312del