Canonical Allele Identifier: PA2825480003
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 240715
ClinVar RCV Id: RCV000234605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Gly1813Cys
CA1938381
NM_001081676.2:c.5437G>T