Canonical Allele Identifier: PA2827383819
Gene: CBX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 161834
ClinVar RCV Id: RCV000149370

Amino-acid Alleles

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