Canonical Allele Identifier: PA2826128765
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1024408
ClinVar RCV Id: RCV001841210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Glu50Lys
CA397994236
NM_001177801.2:c.148G>A