Canonical Allele Identifier: PA2826832475
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 938804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Arg498Gln
CA2320832
NM_001293306.2:c.1493G>A