Canonical Allele Identifier: PA2827328281
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 666402
ClinVar RCV Id: RCV001842005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317056.1:p.Ile17Asn
CA8374287
NM_001330127.2:c.50T>A