Canonical Allele Identifier: PA2827328349
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2047768
ClinVar RCV Id: RCV002918291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317056.1:p.Gly60Asp
CA397994404
NM_001330127.2:c.179G>A