Canonical Allele Identifier: PA2827776426
Gene: SCN1A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Leu851Trp
CA303139
NM_001353954.2:c.2552T>G