Canonical Allele Identifier: PA645458908
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_008853.3:p.Gly1862Cys
CA1938381
NM_006922.4:c.5584G>T