Canonical Allele Identifier: PA2826004479
Gene: DCAF17 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717639
ClinVar RCV Id: RCV002296518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158293.1:p.Met88Leu
CA349276407
NM_001164821.2:c.262A>C
CA349276409
NM_001164821.2:c.262A>T