Canonical Allele Identifier: PA658828014
Gene: RAD21 HGNC NCBI

Linked Data

ClinVar Variation Id: 560415
ClinVar RCV Id: RCV000678504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006256.1:p.Ala622Thr
CA4852673
NM_006265.3:c.1864G>A