Canonical Allele Identifier: PA2826128768
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 3151481
ClinVar RCV Id: RCV004445870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Glu53Gly
CA8374329
NM_001177801.2:c.158A>G