Canonical Allele Identifier: PA2826139169
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Ala473Thr
CA7988675
NM_001178098.2:c.1417G>A