Canonical Allele Identifier: PA2828437968
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2419938
ClinVar RCV Id: RCV003118463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357464.1:p.Val576Leu
CA8169093
NM_001370535.1:c.1726G>C
CA396760172
NM_001370535.1:c.1726G>T