Canonical Allele Identifier: PA239881
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 194080
ClinVar RCV Id: RCV000174357 RCV000858470 RCV004537364 RCV002517674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Ser540Phe
CA239880
NM_006922.4:c.1619C>T