Canonical Allele Identifier: PA2826128775
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 543067
ClinVar RCV Id: RCV001841850 RCV004025913 RCV001766422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Val58Ile
CA8374335
NM_001177801.2:c.172G>A