Canonical Allele Identifier: PA916071492
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996784.1:p.Gly50Ser
CA9516064
NM_206901.3:c.148G>A