Canonical Allele Identifier: PA2573249422
Gene: RAD21 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356689
ClinVar RCV Id: RCV001870219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006256.1:p.Ile621Met
CA371988726
NM_006265.3:c.1863C>G