Canonical Allele Identifier: PA2828439238
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2149749
ClinVar RCV Id: RCV003083245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357471.1:p.Tyr177Cys
CA8169239
NM_001370542.1:c.530A>G