Canonical Allele Identifier: PA2825478978
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 431726
ClinVar RCV Id: RCV000655959 RCV001856998 RCV002250643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075145.1:p.Leu209Pro
CA349239608
NM_001081676.2:c.626T>C