Canonical Allele Identifier: PA2827788749
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1310712
ClinVar RCV Id: RCV001767826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Phe1152Ser
CA349056570
NM_001353960.2:c.3455T>C