Canonical Allele Identifier: PA2573221932
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1410107
ClinVar RCV Id: RCV001940005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001761.3:p.Tyr461Cys
CA395406534
NM_001770.6:c.1382A>G