Canonical Allele Identifier: PA915987513
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 646578
ClinVar RCV Id: RCV000800894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Asp1374Val
CA1938644
NM_006922.4:c.4121A>T