Canonical Allele Identifier: PA2828437957
Gene: RFWD3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357464.1:p.Ile564Val
CA8169109
NM_001370535.1:c.1690A>G