Canonical Allele Identifier: PA2580335688
Gene: RAD21 HGNC NCBI

Linked Data

ClinVar Variation Id: 2086083
ClinVar RCV Id: RCV003015396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006256.1:p.Ala576Val
CA4852689
NM_006265.3:c.1727C>T