Canonical Allele Identifier: PA2580257514
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920790
ClinVar RCV Id: RCV002591302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Val472Phe
CA395406681
NM_001770.6:c.1414G>T