Canonical Allele Identifier: PA215916
Gene: CDC73 HGNC NCBI

Linked Data

ClinVar Variation Id: 41848
ClinVar RCV Id: RCV000034781 RCV000473561 RCV002381287 RCV003460547 RCV002482952 RCV003153326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078805.3:p.Met435Thr
CA215914
NM_024529.5:c.1304T>C