Canonical Allele Identifier: PA2827775386
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Pro113Thr
CA303135
NM_001353954.2:c.337C>A