Canonical Allele Identifier: PA2828437578
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2871542
ClinVar RCV Id: RCV003698541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357463.1:p.Thr572Met
CA8169096
NM_001370534.1:c.1715C>T