Canonical Allele Identifier: PA2827788042
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2047965
ClinVar RCV Id: RCV002926987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg616Lys
CA349067454
NM_001353960.2:c.1847G>A