Canonical Allele Identifier: PA2573267504
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1403512
ClinVar RCV Id: RCV001909093
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Arg59Pro
CA397994394
NM_016492.5:c.176G>C