Canonical Allele Identifier: PA2826128861
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2808825
ClinVar RCV Id: RCV003755380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171273.1:p.Ala56Asp
CA397994353
NM_001177802.2:c.167C>A