Canonical Allele Identifier: PA2573088572
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 842350
ClinVar RCV Id: RCV001044755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Pro510Leu
CA2320817
NM_006514.4:c.1529C>T