Canonical Allele Identifier: PA2826139047
Gene: CD19 HGNC NCBI

Linked Data

ClinVar Variation Id: 318804
ClinVar RCV Id: RCV000366349 RCV000662337 RCV004021653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171569.1:p.Pro176Leu
CA7988382
NM_001178098.2:c.527C>T