Canonical Allele Identifier: PA107833
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ile252Asn
CA285255
NM_001165963.4:c.755T>A