Canonical Allele Identifier: PA2828439052
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2004368
ClinVar RCV Id: RCV002816047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357469.1:p.Thr294Arg
CA396760198
NM_001370540.1:c.881C>G