Allele Registry

Canonical Allele Identifier: PA2829530900

Gene: BCR HGNC NCBI

ClinVar RCV:

RCV001540040

ClinVar Variation:

1182413

HGVS (amino-acid)	Matching Registered Transcripts
NP_004318.3:p.Asn796Ser	CA10142571 NM_004327.4:c.2387A>G