Canonical Allele Identifier: PA2826832469
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 407757
ClinVar RCV Id: RCV000466931 RCV002393114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Lys496Glu
CA2320837
NM_001293306.2:c.1486A>G