Canonical Allele Identifier: PA2573211237
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1384443
ClinVar RCV Id: RCV001896001 RCV003148998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asn1391Asp
CA349063320
NM_001365536.1:c.4171A>G