Canonical Allele Identifier: PA2827774915
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Met1769Thr
CA285018
NM_001353952.2:c.5306T>C