Canonical Allele Identifier: PA2828439229
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1977557
ClinVar RCV Id: RCV002774835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357471.1:p.Lys162Asn
CA8169251
NM_001370542.1:c.486G>C
CA396761775
NM_001370542.1:c.486G>T