Canonical Allele Identifier: PA302118
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 190841
ClinVar RCV Id: RCV001711343 RCV001842510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Leu18Phe
CA302117
NM_016492.5:c.52C>T