Canonical Allele Identifier: PA2827777320
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Pro1439Thr
CA303087
NM_001353954.2:c.4315C>A