Canonical Allele Identifier: PA2827774053
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2704798
ClinVar RCV Id: RCV003589804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ser1284Ala
CA349053533
NM_001353952.2:c.3850T>G