Canonical Allele Identifier: PA1139734416
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 958488
ClinVar RCV Id: RCV001231666
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ala1484Glu
CA349058269
NM_001365536.1:c.4451C>A