Canonical Allele Identifier: PA2827774088
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1385928
ClinVar RCV Id: RCV001889064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Leu1307Val
CA349053111
NM_001353952.2:c.3919C>G