Canonical Allele Identifier: PA2573267502
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1427445
ClinVar RCV Id: RCV001964616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Leu52Pro
CA397994272
NM_016492.5:c.155T>C