Canonical Allele Identifier: PA2741933674
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2702207
ClinVar RCV Id: RCV003577251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Val1329Ala
CA349026044
NM_006922.4:c.3986T>C