Canonical Allele Identifier: PA2499274202
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1015057
ClinVar RCV Id: RCV001313872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Thr574Ile
CA352167133
NM_006514.4:c.1721C>T