Canonical Allele Identifier: PA645458891
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 373960
ClinVar RCV Id: RCV000415038 RCV000494116 RCV000625712 RCV001199328 RCV003243119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008853.3:p.Ile875Thr
CA16043377
NM_006922.4:c.2624T>C