Canonical Allele Identifier: PA2829669011
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1921410
ClinVar RCV Id: RCV002608852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Ser1047Asn
CA2320341
NM_006514.4:c.3140G>A