Canonical Allele Identifier: PA2825480478
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 403867
ClinVar RCV Id: RCV000465765 RCV004022542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075146.1:p.Arg563Cys
CA1939100
NM_001081677.2:c.1687C>T