Canonical Allele Identifier: PA645470040
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005610.1:p.Gly390Ser
CA9516064
NM_005619.5:c.1168G>A