Canonical Allele Identifier: PA2827756875
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Pro358Thr
CA284856
NM_001353949.2:c.1072C>A