Canonical Allele Identifier: PA2826128766
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 190844
ClinVar RCV Id: RCV000171021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Leu51Val
CA302123
NM_001177801.2:c.151C>G