Canonical Allele Identifier: PA2580411386
Gene: RANGRF HGNC NCBI

Linked Data

ClinVar Variation Id: 2255595
ClinVar RCV Id: RCV003108177 RCV004108342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057576.2:p.Ala56Val
CA397994358
NM_016492.5:c.167C>T