Canonical Allele Identifier: PA2827763069
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ile252Asn
CA285255
NM_001353950.2:c.755T>A