Canonical Allele Identifier: PA2499282756
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1024408
ClinVar RCV Id: RCV001841210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Glu50Lys
CA397994236
NM_016492.5:c.148G>A