Canonical Allele Identifier: PA2828439439
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3153440
ClinVar RCV Id: RCV004446341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357472.1:p.Ser130Gly
CA396762182
NM_001370543.1:c.388A>G