Canonical Allele Identifier: PA2573267495
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1430927
ClinVar RCV Id: RCV001971948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Met20Thr
CA287553835
NM_016492.5:c.59T>C