Canonical Allele Identifier: PA2741853375
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2625775
ClinVar RCV Id: RCV003387221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Ser955Tyr
CA2320335
NM_001293307.2:c.2864C>A