Canonical Allele Identifier: PA916071489
Gene: RTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380937
ClinVar RCV Id: RCV000445188 RCV000633075 RCV001848758
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996783.1:p.Phe264Leu
CA9516184
NM_206900.3:c.792C>A
CA406360250
NM_206900.3:c.792C>G
CA406360261
NM_206900.3:c.790T>C