Canonical Allele Identifier: PA2825480911
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 403865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075146.1:p.Gly1281Glu
CA16610166
NM_001081677.2:c.3842G>A