Canonical Allele Identifier: PA916045317
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 94089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met943Leu
CA147603
NM_001365536.1:c.2827A>C
CA349077105
NM_001365536.1:c.2827A>T