Canonical Allele Identifier: PA2580311038
Gene: BCL7C HGNC NCBI
ClinVar Allele:
2317951
ClinVar RCV:
RCV004177074
ClinVar Variation:
2332521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004756.2:p.Ile25Val
CA8015415
NM_004765.4:c.73A>G