Canonical Allele Identifier: PA645458903
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 432534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Arg1621Gln
CA349018276
NM_006922.4:c.4862G>A