Canonical Allele Identifier: PA2828439051
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2871542
ClinVar RCV Id: RCV003698541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357469.1:p.Thr294Met
CA8169096
NM_001370540.1:c.881C>T