Canonical Allele Identifier: PA2829040163
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Ala384Thr
CA7988675
NM_001385732.1:c.1150G>A