Canonical Allele Identifier: PA2826011683
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ile252Asn
CA285255
NM_001165964.3:c.755T>A