Canonical Allele Identifier: PA2828437966
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2871542
ClinVar RCV Id: RCV003698541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357464.1:p.Thr572Met
CA8169096
NM_001370535.1:c.1715C>T