Canonical Allele Identifier: PA645510654
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 439464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Tyr378Ser
CA395405646
NM_001770.6:c.1133A>C