Canonical Allele Identifier: PA645470031
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380937
ClinVar RCV Id: RCV000445188 RCV000633075 RCV001848758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005610.1:p.Phe264Leu
CA9516184
NM_005619.5:c.792C>A
CA406360250
NM_005619.5:c.792C>G
CA406360261
NM_005619.5:c.790T>C