Canonical Allele Identifier: PA2828437913
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079375
ClinVar RCV Id: RCV002995326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357464.1:p.Ile464Val
CA283745759
NM_001370535.1:c.1390A>G