Canonical Allele Identifier: PA916058610
Gene: BCR HGNC NCBI

Linked Data

ClinVar Variation Id: 218629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067585.2:p.Val949Ile
CA249392
NM_021574.3:c.2845G>A