Canonical Allele Identifier: PA2827328293
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2273252
ClinVar RCV Id: RCV004124096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317056.1:p.Ser26Arg
CA397993916
NM_001330127.2:c.76A>C
CA397993972
NM_001330127.2:c.78C>A
CA397993974
NM_001330127.2:c.78C>G