Canonical Allele Identifier: PA1139734353
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys1480del
CA10612802
NM_001365536.1:c.4437_4439del