Canonical Allele Identifier: PA2827774660
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206854
ClinVar RCV Id: RCV000188988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Arg1637Leu
CA317561
NM_001353952.2:c.4910G>T