Canonical Allele Identifier: PA2499282755
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1039994
ClinVar RCV Id: RCV001841211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Thr43Met
CA8374324
NM_016492.5:c.128C>T