Canonical Allele Identifier: PA658816241
Gene: RANBP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 537216
ClinVar RCV Id: RCV000646011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006258.3:p.Glu2637Asp
CA53459463
NM_006267.5:c.7911A>T
CA348082193
NM_006267.5:c.7911A>C