Canonical Allele Identifier: PA2573221934
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Ala473Thr
CA7988675
NM_001770.6:c.1417G>A