Canonical Allele Identifier: PA2829040168
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1955916
ClinVar RCV Id: RCV002695750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372661.1:p.Asp398Tyr
CA7988696
NM_001385732.1:c.1192G>T