Canonical Allele Identifier: PA2827753055
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 444532
ClinVar RCV Id: RCV000512678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Leu1309Arg
CA349053253
NM_001353948.2:c.3926T>G