Canonical Allele Identifier: PA2573211196
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1398703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu1295Val
CA349066423
NM_001365536.1:c.3883T>G