Canonical Allele Identifier: PA2830513217
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996783.1:p.Gly317Ser
CA9516064
NM_206900.3:c.949G>A