Canonical Allele Identifier: PA2826128779
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 1403512
ClinVar RCV Id: RCV001909093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171272.1:p.Arg59Pro
CA397994394
NM_001177801.2:c.176G>C