Canonical Allele Identifier: PA111401
Gene: EZH2 HGNC NCBI
ClinVar Allele:
39156
ClinVar RCV:
RCV000023119
ClinVar Variation:
30200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001190176.1:p.Pro132Ser
CA259762
NM_001203247.2:c.394C>T