Canonical Allele Identifier: PA2826128753
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2092901
ClinVar RCV Id: RCV003008328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Val31Gly
CA397994015
NM_001177801.2:c.92T>G