Canonical Allele Identifier: PA2826128759
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1039994
ClinVar RCV Id: RCV001841211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Thr43Met
CA8374324
NM_001177801.2:c.128C>T