Canonical Allele Identifier: PA645375775
Gene: DCAF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 373149
ClinVar RCV Id: RCV000413871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056541.2:p.Thr51Ile
CA16042299
NM_015726.4:c.152C>T