Canonical Allele Identifier: PA2830245804
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 138873
ClinVar RCV Id: RCV000128967 RCV000212967 RCV000588832 RCV001354814 RCV001723701 RCV000203773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598332.1:p.Glu121Gly
CA293923
NM_133629.3:c.362A>G