Canonical Allele Identifier: PA2826832928
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 240667
ClinVar RCV Id: RCV000226123 RCV000430868 RCV002321881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Pro1044Thr
CA2320343
NM_001293306.2:c.3130C>A