Canonical Allele Identifier: PA2828438292
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2484781
ClinVar RCV Id: RCV004278858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357465.1:p.Arg451Leu
CA396761634
NM_001370536.1:c.1352G>T