Canonical Allele Identifier: PA2829669028
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 576536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Thr1064Met
CA2320325
NM_006514.4:c.3191C>T