Canonical Allele Identifier: PA2825480942
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 657113
ClinVar RCV Id: RCV000813670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075146.1:p.Arg1343Trp
CA349025295
NM_001081677.2:c.4027C>T