Canonical Allele Identifier: PA2828180383
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2499878
ClinVar RCV Id: RCV003223970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu430Ile
CA349085699
NM_001365536.1:c.1288C>A