Canonical Allele Identifier: PA2573211194
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1502601
ClinVar RCV Id: RCV002022418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ala1294Val
CA349066425
NM_001365536.1:c.3881C>T