Canonical Allele Identifier: PA1139728062
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 944744
ClinVar RCV Id: RCV001841186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Ile48Thr
CA397994212
NM_016492.5:c.143T>C