Canonical Allele Identifier: PA916045256
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 471094
ClinVar RCV Id: RCV000528338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Cys710Arg
CA1944325
NM_001365536.1:c.2128T>C