Canonical Allele Identifier: PA2825479198
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 194080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Ser540Phe
CA239880
NM_001081676.2:c.1619C>T