This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA157272
Gene: BCL6 HGNC NCBI
ClinVar RCV:
RCV000120199
ClinVar Variation:
133671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001697.2:p.Glu302Gly
CA157271
NM_001706.5:c.905A>G