Canonical Allele Identifier: PA2827785914
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2430162
ClinVar RCV Id: RCV003128168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Leu1237Met
CA349054328
NM_001353958.2:c.3709C>A