Canonical Allele Identifier: PA2825480646
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 373960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075146.1:p.Ile826Thr
CA16043377
NM_001081677.2:c.2477T>C