Canonical Allele Identifier: PA354804
Gene: BCR HGNC NCBI

Linked Data

ClinVar Variation Id: 218629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004318.3:p.Val949Ile
CA249392
NM_004327.4:c.2845G>A