Canonical Allele Identifier: PA2826834855
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2563715
ClinVar RCV Id: RCV003306044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Ala1550Thr
CA2319775
NM_001293307.2:c.4648G>A