Canonical Allele Identifier: PA2828439511
Gene: RFWD3 HGNC NCBI
ClinVar RCV:
RCV003035747
ClinVar Variation:
2124096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357472.1:p.Ile286Val
CA8169109
NM_001370543.1:c.856A>G