Canonical Allele Identifier: PA2828438999
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_001357469.1:p.Ile186Val
CA283745759
NM_001370540.1:c.556A>G