Canonical Allele Identifier: PA2827764846
Gene: SCN1A HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Leu852Trp
CA303139
NM_001353950.2:c.2555T>G