Canonical Allele Identifier: PA916045320
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 572991
ClinVar RCV Id: RCV000694527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asp974Glu
CA1944165
NM_001365536.1:c.2922C>G
CA59791845
NM_001365536.1:c.2922C>A