Canonical Allele Identifier: PA2825479701
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 646578
ClinVar RCV Id: RCV000800894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Asp1325Val
CA1938644
NM_001081676.2:c.3974A>T