Canonical Allele Identifier: PA645470033
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 329550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005610.1:p.Ser329Asn
CA9516115
NM_005619.5:c.986G>A