Canonical Allele Identifier: PA2829040127
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 439464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Tyr289Ser
CA395405646
NM_001385732.1:c.866A>C