Canonical Allele Identifier: PA2828438281
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2174994
ClinVar RCV Id: RCV002588308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357465.1:p.Ser425Leu
CA396761990
NM_001370536.1:c.1274C>T