Canonical Allele Identifier: PA2573252023
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1359935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Pro550Leu
CA352167293
NM_006514.4:c.1649C>T