Canonical Allele Identifier: PA2826725165
Gene: BCL7C HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273455.1:p.Ile25Val
CA8015415
NM_001286526.2:c.73A>G