Canonical Allele Identifier: PA2826832483
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 966098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Arg508Gln
CA2320823
NM_001293306.2:c.1523G>A