Canonical Allele Identifier: PA2827777711
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1475981
ClinVar RCV Id: RCV002008007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Leu1665Phe
CA349069620
NM_001353954.2:c.4993C>T