Canonical Allele Identifier: PA2828180388
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2088447
ClinVar RCV Id: RCV003002909
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Glu438Asp
CA349085563
NM_001365536.1:c.1314G>T
CA349085565
NM_001365536.1:c.1314G>C