Canonical Allele Identifier: PA2826128747
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1430927
ClinVar RCV Id: RCV001971948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Met20Thr
CA287553835
NM_001177801.2:c.59T>C