Canonical Allele Identifier: PA2829669033
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3225645
ClinVar RCV Id: RCV004516927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Val1073Ile
CA352156595
NM_006514.4:c.3217G>A