Canonical Allele Identifier: PA2828439299
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2419938
ClinVar RCV Id: RCV003118463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357471.1:p.Val298Leu
CA8169093
NM_001370542.1:c.892G>C
CA396760172
NM_001370542.1:c.892G>T