Canonical Allele Identifier: PA2827383819
Gene: CBX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 161834
ClinVar RCV Id: RCV000149370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333672.1:p.Pro76Arg
CA174874
NM_001346743.1:c.227C>G