Canonical Allele Identifier: PA2827784355
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 848680
ClinVar RCV Id: RCV001052491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Val126Ala
CA349076768
NM_001353958.2:c.377T>C