Canonical Allele Identifier: PA2827328298
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2092901
ClinVar RCV Id: RCV003008328
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317056.1:p.Val31Gly
CA397994015
NM_001330127.2:c.92T>G