Canonical Allele Identifier: PA2829669029
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1932334
ClinVar RCV Id: RCV002622513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Asp1067Glu
CA352156629
NM_006514.4:c.3201T>G
CA352156630
NM_006514.4:c.3201T>A