Canonical Allele Identifier: PA658670691
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448173
ClinVar RCV Id: RCV000517182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005610.1:p.Val456Met
CA9516004
NM_005619.5:c.1366G>A