Canonical Allele Identifier: PA2580462083
Gene: CDC73 HGNC NCBI

Linked Data

ClinVar Variation Id: 2115067
ClinVar RCV Id: RCV003046269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078805.3:p.Thr199Ser
CA343962442
NM_024529.5:c.595A>T
CA343962445
NM_024529.5:c.596C>G