Canonical Allele Identifier: PA2573210962
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1467887
ClinVar RCV Id: RCV001968722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met932Ile
CA349077368
NM_001365536.1:c.2796G>T
CA349077369
NM_001365536.1:c.2796G>C
CA349077371
NM_001365536.1:c.2796G>A