Canonical Allele Identifier: PA916053125
Gene: DCAF17 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079276.2:p.Asn32Thr
CA1964543
NM_025000.4:c.95A>C