Canonical Allele Identifier: PA2573267507
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1507967
ClinVar RCV Id: RCV002013717
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Ala62Gly
CA397994430
NM_016492.5:c.185C>G