Canonical Allele Identifier: PA2741958526
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2721486
ClinVar RCV Id: RCV003592921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Val58Glu
CA397994386
NM_016492.5:c.173T>A