Canonical Allele Identifier: PA2827780829
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1519829
ClinVar RCV Id: RCV002043796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Asn1735Lys
CA349068416
NM_001353955.2:c.5205C>A
CA349068418
NM_001353955.2:c.5205C>G