Canonical Allele Identifier: PA2825479942
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 521063
ClinVar RCV Id: RCV000622981 RCV000625714 RCV003992349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Val1720Ala
CA349016016
NM_001081676.2:c.5159T>C