Canonical Allele Identifier: PA2828180199
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1009477
ClinVar RCV Id: RCV001306971 RCV002545001
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile239Val
CA349093184
NM_001365536.1:c.715A>G