Canonical Allele Identifier: PA2826834416
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 373671
ClinVar RCV Id: RCV000413612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Pro1004Ser
CA16042470
NM_001293307.2:c.3010C>T